WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.113367766C>G , CM000666.2:g.113367766C>G | GRCh38 |
| NC_000004.11:g.114288922C>G , CM000666.1:g.114288922C>G | GRCh37 |
| NC_000004.10:g.114508371C>G | NCBI36 |
| NG_009006.2:g.554684C>G , LRG_327:g.554684C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000506344.6:c.11374C>G | ENSP00000422888.2:p.His3792Asp | |
| ENST00000705785.1:c.5059C>G | ENSP00000516169.1:p.His1687Asp | |
| ENST00000510275.8:c.1660C>G | ENSP00000421023.4:p.His554Asp | |
| ENST00000612754.2:c.2158C>G | ENSP00000482888.2:p.His720Asp | |
| ENST00000681990.1:n.2615C>G | ||
| ENST00000682049.1:n.1823C>G | ||
| ENST00000682959.1:n.2567C>G | ||
| ENST00000683389.1:n.1396C>G | ||
| ENST00000683826.1:n.3358C>G | ||
| ENST00000683893.1:n.1339C>G | ||
| ENST00000683908.1:n.1732C>G | ||
| ENST00000683972.1:n.8078C>G | ||
| ENST00000684225.1:n.2704C>G | ||
| ENST00000684378.1:n.688C>G | ||
| ENST00000684470.1:n.3122C>G | ||
| ENST00000684730.1:n.1337C>G | ||
| ENST00000357077.9:c.11233C>G MANE Select | ENSP00000349588.4:p.His3745Asp | |
| ENST00000503423.6:c.11071C>G | ENSP00000421011.2:p.His3691Asp | |
| ENST00000505342.6:c.2365C>G | ENSP00000422498.2:p.His789Asp | |
| ENST00000510275.7:c.688C>G | ENSP00000421023.3:p.His230Asp | |
| ENST00000671704.1:c.4792C>G | ENSP00000500926.1:p.His1598Asp | |
| ENST00000671727.1:c.4879C>G | ENSP00000500102.1:p.His1627Asp | |
| ENST00000671756.1:c.4816C>G | ENSP00000500712.1:p.His1606Asp | |
| ENST00000671762.1:c.5014C>G | ENSP00000500954.1:p.His1672Asp | |
| ENST00000671793.1:c.4915C>G | ENSP00000499928.1:p.His1639Asp | |
| ENST00000671809.1:c.11107C>G | ENSP00000500872.1:p.His3703Asp | |
| ENST00000671825.1:c.4915C>G | ENSP00000500459.1:p.His1639Asp | |
| ENST00000671854.1:c.4717C>G | ENSP00000500833.1:p.His1573Asp | |
| ENST00000671863.1:c.*471C>G | ENSP00000500855.1:n.*471C>G | |
| ENST00000671882.1:c.11050C>G | ENSP00000499887.1:p.His3684Asp | |
| ENST00000671893.1:c.4594C>G | ENSP00000499986.1:p.His1532Asp | |
| ENST00000671906.1:c.11047C>G | ENSP00000499953.1:p.His3683Asp | |
| ENST00000671951.1:c.4693C>G | ENSP00000500528.1:p.His1565Asp | |
| ENST00000671971.1:c.11278C>G | ENSP00000499832.1:p.His3760Asp | |
| ENST00000672045.1:c.4816C>G | ENSP00000499959.1:p.His1606Asp | |
| ENST00000672068.1:c.11071C>G | ENSP00000499902.1:p.His3691Asp | |
| ENST00000672088.1:c.4792C>G | ENSP00000499837.1:p.His1598Asp | |
| ENST00000672090.1:c.11071C>G | ENSP00000500540.1:p.His3691Asp | |
| ENST00000672177.1:c.4828C>G | ENSP00000500918.1:p.His1610Asp | |
| ENST00000672209.1:c.11071C>G | ENSP00000499982.1:p.His3691Asp | |
| ENST00000672221.1:c.4813C>G | ENSP00000500473.1:p.His1605Asp | |
| ENST00000672240.1:c.11314C>G | ENSP00000500548.1:p.His3772Asp | |
| ENST00000672246.1:c.4801C>G | ENSP00000499990.1:p.His1601Asp | |
| ENST00000672251.1:c.11035C>G | ENSP00000500580.1:p.His3679Asp | |
| ENST00000672312.1:c.4816C>G | ENSP00000500378.1:p.His1606Asp | |
| ENST00000672315.1:c.4915C>G | ENSP00000500780.1:p.His1639Asp | |
| ENST00000672350.1:c.4753C>G | ENSP00000500420.1:p.His1585Asp | |
| ENST00000672356.1:c.4693C>G | ENSP00000500544.1:p.His1565Asp | |
| ENST00000672362.1:c.4951C>G | ENSP00000500522.1:p.His1651Asp | |
| ENST00000672366.1:c.4879C>G | ENSP00000500937.1:p.His1627Asp | |
| ENST00000672402.1:c.4915C>G | ENSP00000500881.1:p.His1639Asp | |
| ENST00000672411.1:c.2542C>G | ENSP00000499979.1:p.His848Asp | |
| ENST00000672502.1:c.11134C>G | ENSP00000499870.1:p.His3712Asp | |
| ENST00000672684.1:c.4717C>G | ENSP00000499943.1:p.His1573Asp | |
| ENST00000672696.1:c.4915C>G | ENSP00000499828.1:p.His1639Asp | |
| ENST00000672731.1:c.4792C>G | ENSP00000500908.1:p.His1598Asp | |
| ENST00000672759.1:c.4693C>G | ENSP00000499881.1:p.His1565Asp | |
| ENST00000672779.1:c.5023C>G | ENSP00000499869.1:p.His1675Asp | |
| ENST00000672793.1:c.4816C>G | ENSP00000500150.1:p.His1606Asp | |
| ENST00000672830.1:c.11170C>G | ENSP00000500222.1:p.His3724Asp | |
| ENST00000672854.1:c.4780C>G | ENSP00000500311.1:p.His1594Asp | |
| ENST00000672880.1:c.4816C>G | ENSP00000500866.1:p.His1606Asp | |
| ENST00000672915.1:c.2365C>G | ENSP00000500622.1:p.His789Asp | |
| ENST00000672930.1:c.11071C>G | ENSP00000499913.1:p.His3691Asp | |
| ENST00000672934.1:c.10972C>G | ENSP00000500645.1:p.His3658Asp | |
| ENST00000672955.1:c.4792C>G | ENSP00000500527.1:p.His1598Asp | |
| ENST00000672965.1:c.4852C>G | ENSP00000499891.1:p.His1618Asp | |
| ENST00000672986.1:c.4396C>G | ENSP00000499967.1:p.His1466Asp | |
| ENST00000672990.1:c.4852C>G | ENSP00000500275.1:p.His1618Asp | |
| ENST00000673044.1:c.4915C>G | ENSP00000500933.1:p.His1639Asp | |
| ENST00000673048.1:c.2527C>G | ENSP00000500832.1:p.His843Asp | |
| ENST00000673109.1:c.10948C>G | ENSP00000500265.1:p.His3650Asp | |
| ENST00000673231.1:c.2542C>G | ENSP00000500111.1:p.His848Asp | |
| ENST00000673240.1:c.5023C>G | ENSP00000499996.1:p.His1675Asp | |
| ENST00000673255.1:c.4816C>G | ENSP00000500423.1:p.His1606Asp | |
| ENST00000673298.1:c.11071C>G | ENSP00000500245.1:p.His3691Asp | |
| ENST00000673334.1:c.11071C>G | ENSP00000500854.1:p.His3691Asp | |
| ENST00000673353.1:c.2506C>G | ENSP00000500007.1:p.His836Asp | |
| ENST00000673363.1:c.11179C>G | ENSP00000500539.1:p.His3727Asp | |
| ENST00000673430.1:c.4816C>G | ENSP00000500269.1:p.His1606Asp | |
| ENST00000673453.1:c.4744C>G | ENSP00000500112.1:p.His1582Asp | |
| ENST00000673536.1:c.4486C>G | ENSP00000500524.1:p.His1496Asp | |
| ENST00000673538.1:c.*471C>G | ENSP00000500842.1:n.*471C>G | |
| ENST00000673546.1:c.4753C>G | ENSP00000500843.1:p.His1585Asp | |
| ENST00000673555.1:c.11071C>G | ENSP00000500947.1:p.His3691Asp | |
| ENST00000673573.1:c.11008C>G | ENSP00000500883.1:p.His3670Asp | |
| ENST00000264366.10:c.11134C>G | ENSP00000264366.6:p.His3712Asp | |
| ENST00000357077.8:c.11233C>G | ENSP00000349588.4:p.His3745Asp | |
| ENST00000394537.7:c.4978C>G | ENSP00000378044.3:p.His1660Asp | |
| ENST00000505342.5:c.2263C>G | ENSP00000422498.1:p.His755Asp | |
| ENST00000506722.5:c.4951C>G | ENSP00000421067.1:p.His1651Asp | |
| ENST00000509550.5:c.2506C>G | ENSP00000426944.1:p.His836Asp | |
| ENST00000510275.6:c.934C>G | ENSP00000421023.2:p.His312Asp | |
| ENST00000514960.5:c.1982C>G | ||
| ENST00000612754.1:c.*2594C>G | ENSP00000482888.1:n.*2594C>G | |
| NM_001127493.1:c.4951C>G , LRG_327t2:c.4951C>G | NP_001120965.1:p.His1651Asp | |
| NM_001148.4:c.11233C>G , LRG_327t1:c.11233C>G | NP_001139.3:p.His3745Asp | |
| NM_020977.3:c.4978C>G | NP_066187.2:p.His1660Asp | |
| XM_005262942.3:c.11266C>G | XP_005262999.1:p.His3756Asp | |
| XM_005262945.1:c.11134C>G | XP_005263002.1:p.His3712Asp | |
| XM_005262948.3:c.4975C>G | XP_005263005.1:p.His1659Asp | |
| XM_006714188.2:c.11320C>G | XP_006714251.1:p.His3774Asp | |
| XM_006714189.2:c.11284C>G | XP_006714252.1:p.His3762Asp | |
| XM_006714190.2:c.5032C>G | XP_006714253.1:p.His1678Asp | |
| XM_006714191.2:c.5065C>G | XP_006714254.1:p.His1689Asp | |
| XM_006714192.2:c.4996C>G | XP_006714255.1:p.His1666Asp | |
| XM_006714193.2:c.5065C>G | XP_006714256.1:p.His1689Asp | |
| XM_006714194.2:c.11260C>G | XP_006714257.1:p.His3754Asp | |
| XM_011531891.1:c.11305C>G | XP_011530193.1:p.His3769Asp | |
| NM_001127493.2:c.4951C>G | NP_001120965.1:p.His1651Asp | |
| NM_001148.5:c.11233C>G | NP_001139.3:p.His3745Asp | |
| NM_001354225.1:c.4990C>G | NP_001341154.1:p.His1664Asp | |
| NM_001354228.1:c.4879C>G | NP_001341157.1:p.His1627Asp | |
| NM_001354230.1:c.4957C>G | NP_001341159.1:p.His1653Asp | |
| NM_001354231.1:c.5020C>G | NP_001341160.1:p.His1674Asp | |
| NM_001354232.1:c.5014C>G | NP_001341161.1:p.His1672Asp | |
| NM_001354235.1:c.4975C>G | NP_001341164.1:p.His1659Asp | |
| NM_001354236.1:c.4876C>G | NP_001341165.1:p.His1626Asp | |
| NM_001354237.1:c.5056C>G | NP_001341166.1:p.His1686Asp | |
| NM_001354239.1:c.4948C>G | NP_001341168.1:p.His1650Asp | |
| NM_001354240.1:c.5023C>G | NP_001341169.1:p.His1675Asp | |
| NM_001354241.1:c.5023C>G | NP_001341170.1:p.His1675Asp | |
| NM_001354242.1:c.5020C>G | NP_001341171.1:p.His1674Asp | |
| NM_001354243.1:c.4915C>G | NP_001341172.1:p.His1639Asp | |
| NM_001354244.1:c.4912C>G | NP_001341173.1:p.His1638Asp | |
| NM_001354245.1:c.4816C>G | NP_001341174.1:p.His1606Asp | |
| NM_001354246.1:c.4975C>G | NP_001341175.1:p.His1659Asp | |
| NM_001354249.1:c.4792C>G | NP_001341178.1:p.His1598Asp | |
| NM_001354252.1:c.4948C>G | NP_001341181.1:p.His1650Asp | |
| NM_001354253.1:c.4753C>G | NP_001341182.1:p.His1585Asp | |
| NM_001354254.1:c.4927C>G | NP_001341183.1:p.His1643Asp | |
| NM_001354255.1:c.4915C>G | NP_001341184.1:p.His1639Asp | |
| NM_001354256.1:c.4912C>G | NP_001341185.1:p.His1638Asp | |
| NM_001354257.1:c.4717C>G | NP_001341186.1:p.His1573Asp | |
| NM_001354258.1:c.4879C>G | NP_001341187.1:p.His1627Asp | |
| NM_001354260.1:c.4693C>G | NP_001341189.1:p.His1565Asp | |
| NM_001354261.1:c.4837C>G | NP_001341190.1:p.His1613Asp | |
| NM_001354262.1:c.4816C>G | NP_001341191.1:p.His1606Asp | |
| NM_001354264.1:c.4813C>G | NP_001341193.1:p.His1605Asp | |
| NM_001354265.1:c.4975C>G | NP_001341194.1:p.His1659Asp | |
| NM_001354266.1:c.4792C>G | NP_001341195.1:p.His1598Asp | |
| NM_001354267.1:c.4792C>G | NP_001341196.1:p.His1598Asp | |
| NM_001354268.1:c.4780C>G | NP_001341197.1:p.His1594Asp | |
| NM_001354269.1:c.4765C>G | NP_001341198.1:p.His1589Asp | |
| NM_001354270.1:c.4753C>G | NP_001341199.1:p.His1585Asp | |
| NM_001354271.1:c.4693C>G | NP_001341200.1:p.His1565Asp | |
| NM_001354272.1:c.4849C>G | NP_001341201.1:p.His1617Asp | |
| NM_001354273.1:c.4678C>G | NP_001341202.1:p.His1560Asp | |
| NM_001354274.1:c.4744C>G | NP_001341203.1:p.His1582Asp | |
| NM_001354275.1:c.4816C>G | NP_001341204.1:p.His1606Asp | |
| NM_001354276.1:c.4792C>G | NP_001341205.1:p.His1598Asp | |
| NM_001354277.1:c.4594C>G | NP_001341206.1:p.His1532Asp | |
| NM_001354278.1:c.2506C>G | NP_001341207.1:p.His836Asp | |
| NM_001354279.1:c.2542C>G | NP_001341208.1:p.His848Asp | |
| NM_001354280.1:c.2527C>G | NP_001341209.1:p.His843Asp | |
| NM_001354281.1:c.2506C>G | NP_001341210.1:p.His836Asp | |
| NM_001354282.1:c.2542C>G | NP_001341211.1:p.His848Asp | |
| NM_020977.4:c.4978C>G | NP_066187.2:p.His1660Asp | |
| XM_005262945.3:c.11134C>G | XP_005263002.1:p.His3712Asp | |
| XM_017008067.1:c.11374C>G | XP_016863556.1:p.His3792Asp | |
| XM_017008069.1:c.11350C>G | XP_016863558.1:p.His3784Asp | |
| XM_017008071.2:c.11260C>G | XP_016863560.1:p.His3754Asp | |
| XM_017008072.2:c.11236C>G | XP_016863561.1:p.His3746Asp | |
| XM_017008073.2:c.11233C>G | XP_016863562.1:p.His3745Asp | |
| XM_017008074.2:c.11206C>G | XP_016863563.1:p.His3736Asp | |
| XM_017008075.2:c.11170C>G | XP_016863564.1:p.His3724Asp | |
| XM_017008076.2:c.11233C>G | XP_016863565.1:p.His3745Asp | |
| XM_017008077.2:c.11047C>G | XP_016863566.1:p.His3683Asp | |
| XM_017008078.2:c.4978C>G | XP_016863567.1:p.His1660Asp | |
| XM_017008080.2:c.4828C>G | XP_016863569.1:p.His1610Asp | |
| XM_024454016.1:c.11269C>G | XP_024309784.1:p.His3757Asp | |
| XM_024454017.1:c.5014C>G | XP_024309785.1:p.His1672Asp | |
| XM_024454018.1:c.4879C>G | XP_024309786.1:p.His1627Asp | |
| XM_024454019.1:c.4957C>G | XP_024309787.1:p.His1653Asp | |
| XM_024454020.1:c.4879C>G | XP_024309788.1:p.His1627Asp | |
| XM_024454021.1:c.4876C>G | XP_024309789.1:p.His1626Asp | |
| XM_024454022.1:c.4816C>G | XP_024309790.1:p.His1606Asp | |
| XM_024454023.1:c.4678C>G | XP_024309791.1:p.His1560Asp | |
| NM_001148.6:c.11233C>G MANE Select | NP_001139.3:p.His3745Asp | |
| NM_001127493.3:c.4951C>G | NP_001120965.1:p.His1651Asp | |
| NM_001354225.2:c.4990C>G | NP_001341154.1:p.His1664Asp | |
| NM_001354228.2:c.4879C>G | NP_001341157.1:p.His1627Asp | |
| NM_001354230.2:c.4957C>G | NP_001341159.1:p.His1653Asp | |
| NM_001354231.2:c.5020C>G | NP_001341160.1:p.His1674Asp | |
| NM_001354232.2:c.5014C>G | NP_001341161.1:p.His1672Asp | |
| NM_001354235.2:c.4975C>G | NP_001341164.1:p.His1659Asp | |
| NM_001354236.2:c.4876C>G | NP_001341165.1:p.His1626Asp | |
| NM_001354237.2:c.5056C>G | NP_001341166.1:p.His1686Asp | |
| NM_001354239.2:c.4948C>G | NP_001341168.1:p.His1650Asp | |
| NM_001354240.2:c.5023C>G | NP_001341169.1:p.His1675Asp | |
| NM_001354241.2:c.5023C>G | NP_001341170.1:p.His1675Asp | |
| NM_001354242.2:c.5020C>G | NP_001341171.1:p.His1674Asp | |
| NM_001354243.2:c.4915C>G | NP_001341172.1:p.His1639Asp | |
| NM_001354244.2:c.4912C>G | NP_001341173.1:p.His1638Asp | |
| NM_001354245.2:c.4816C>G | NP_001341174.1:p.His1606Asp | |
| NM_001354246.2:c.4975C>G | NP_001341175.1:p.His1659Asp | |
| NM_001354249.2:c.4792C>G | NP_001341178.1:p.His1598Asp | |
| NM_001354252.2:c.4948C>G | NP_001341181.1:p.His1650Asp | |
| NM_001354253.2:c.4753C>G | NP_001341182.1:p.His1585Asp | |
| NM_001354254.2:c.4927C>G | NP_001341183.1:p.His1643Asp | |
| NM_001354255.2:c.4915C>G | NP_001341184.1:p.His1639Asp | |
| NM_001354256.2:c.4912C>G | NP_001341185.1:p.His1638Asp | |
| NM_001354257.2:c.4717C>G | NP_001341186.1:p.His1573Asp | |
| NM_001354258.2:c.4879C>G | NP_001341187.1:p.His1627Asp | |
| NM_001354260.2:c.4693C>G | NP_001341189.1:p.His1565Asp | |
| NM_001354261.2:c.4837C>G | NP_001341190.1:p.His1613Asp | |
| NM_001354262.2:c.4816C>G | NP_001341191.1:p.His1606Asp | |
| NM_001354264.2:c.4813C>G | NP_001341193.1:p.His1605Asp | |
| NM_001354265.2:c.4975C>G | NP_001341194.1:p.His1659Asp | |
| NM_001354266.2:c.4792C>G | NP_001341195.1:p.His1598Asp | |
| NM_001354267.2:c.4792C>G | NP_001341196.1:p.His1598Asp | |
| NM_001354268.2:c.4780C>G | NP_001341197.1:p.His1594Asp | |
| NM_001354269.3:c.4765C>G | NP_001341198.1:p.His1589Asp | |
| NM_001354270.2:c.4753C>G | NP_001341199.1:p.His1585Asp | |
| NM_001354271.2:c.4693C>G | NP_001341200.1:p.His1565Asp | |
| NM_001354272.2:c.4849C>G | NP_001341201.1:p.His1617Asp | |
| NM_001354273.2:c.4678C>G | NP_001341202.1:p.His1560Asp | |
| NM_001354274.2:c.4744C>G | NP_001341203.1:p.His1582Asp | |
| NM_001354275.2:c.4816C>G | NP_001341204.1:p.His1606Asp | |
| NM_001354276.2:c.4792C>G | NP_001341205.1:p.His1598Asp | |
| NM_001354277.2:c.4594C>G | NP_001341206.1:p.His1532Asp | |
| NM_001354278.2:c.2506C>G | NP_001341207.1:p.His836Asp | |
| NM_001354279.2:c.2542C>G | NP_001341208.1:p.His848Asp | |
| NM_001354280.2:c.2527C>G | NP_001341209.1:p.His843Asp | |
| NM_001354281.2:c.2506C>G | NP_001341210.1:p.His836Asp | |
| NM_001354282.2:c.2542C>G | NP_001341211.1:p.His848Asp | |
| NM_001386142.1:c.10999C>G | NP_001373071.1:p.His3667Asp | |
| NM_001386143.1:c.4915C>G | NP_001373072.1:p.His1639Asp | |
| NM_001386144.1:c.5023C>G | NP_001373073.1:p.His1675Asp | |
| NM_001386146.1:c.4759C>G | NP_001373075.1:p.His1587Asp | |
| NM_001386147.1:c.4804C>G | NP_001373076.1:p.His1602Asp | |
| NM_001386148.2:c.4963C>G | NP_001373077.1:p.His1655Asp | |
| NM_001386149.1:c.4759C>G | NP_001373078.1:p.His1587Asp | |
| NM_001386150.1:c.4759C>G | NP_001373079.1:p.His1587Asp | |
| NM_001386151.1:c.4693C>G | NP_001373080.1:p.His1565Asp | |
| NM_001386152.1:c.5035C>G | NP_001373081.1:p.His1679Asp | |
| NM_001386153.1:c.4759C>G | NP_001373082.1:p.His1587Asp | |
| NM_001386154.1:c.4744C>G | NP_001373083.1:p.His1582Asp | |
| NM_001386156.1:c.4717C>G | NP_001373085.1:p.His1573Asp | |
| NM_001386157.1:c.4594C>G | NP_001373086.1:p.His1532Asp | |
| NM_001386158.1:c.4495C>G | NP_001373087.1:p.His1499Asp | |
| NM_001386160.1:c.4822C>G | NP_001373089.1:p.His1608Asp | |
| NM_001386161.1:c.4912C>G | NP_001373090.1:p.His1638Asp | |
| NM_001386162.1:c.4792C>G | NP_001373091.1:p.His1598Asp | |
| NM_001386166.1:c.7633C>G | NP_001373095.1:p.His2545Asp | |
| NM_001386167.1:c.1378C>G | NP_001373096.1:p.His460Asp | |
| NM_001386174.1:c.11374C>G | NP_001373103.1:p.His3792Asp | |
| NM_001386175.1:c.11350C>G | NP_001373104.1:p.His3784Asp | |
| NM_001386186.2:c.4963C>G | NP_001373115.1:p.His1655Asp | |
| NM_001386187.2:c.4843C>G | NP_001373116.1:p.His1615Asp | |
| NM_020977.5:c.4978C>G | NP_066187.2:p.His1660Asp |