UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2086826T>G , CM000678.2:g.2086826T>G | GRCh38 |
| NC_000016.9:g.2136827T>G , CM000678.1:g.2136827T>G | GRCh37 |
| NC_000016.8:g.2076828T>G | NCBI36 |
| NG_005895.1:g.42521T>G , LRG_487:g.42521T>G | |
| NG_008617.1:g.56395A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3293T>G | ENSP00000455997.2:n.*3293T>G | |
| ENST00000642206.2:c.4791T>G | ENSP00000495146.2:p.Ile1597Met | |
| ENST00000642365.2:c.4941T>G | ENSP00000495459.2:p.Ile1647Met | |
| ENST00000644417.2:c.*5457T>G | ENSP00000493912.2:n.*5457T>G | |
| ENST00000646464.2:c.*7693T>G | ENSP00000496610.2:n.*7693T>G | |
| ENST00000219476.9:c.4944T>G MANE Select | ENSP00000219476.3:p.Ile1648Met | |
| ENST00000350773.9:c.4875T>G | ENSP00000344383.4:p.Ile1625Met | |
| ENST00000401874.7:c.4743T>G | ENSP00000384468.2:p.Ile1581Met | |
| ENST00000568454.6:c.4776T>G | ENSP00000454487.1:p.Ile1592Met | |
| ENST00000569110.2:c.1167T>G | ||
| ENST00000569930.2:n.2826T>G | ||
| ENST00000642365.1:c.3598T>G | ||
| ENST00000642561.1:c.4815T>G | ENSP00000495099.1:p.Ile1605Met | |
| ENST00000642728.1:n.1126T>G | ||
| ENST00000642791.1:n.541T>G | ||
| ENST00000642797.1:c.4746T>G | ENSP00000493846.1:p.Ile1582Met | |
| ENST00000642936.1:c.4812T>G | ENSP00000494514.1:p.Ile1604Met | |
| ENST00000643088.1:c.4737T>G | ENSP00000494747.1:p.Ile1579Met | |
| ENST00000643177.1:n.958T>G | ||
| ENST00000643426.1:n.2592T>G | ||
| ENST00000643946.1:c.4869T>G | ENSP00000495927.1:p.Ile1623Met | |
| ENST00000644043.1:c.4815T>G | ENSP00000496262.1:p.Ile1605Met | |
| ENST00000644278.1:n.426T>G | ||
| ENST00000644329.1:c.4743T>G | ENSP00000496611.1:p.Ile1581Met | |
| ENST00000644335.1:c.4740T>G | ENSP00000496317.1:p.Ile1580Met | |
| ENST00000644399.1:c.4865T>G | ||
| ENST00000645024.1:n.3028T>G | ||
| ENST00000646388.1:c.4938T>G | ENSP00000495921.1:p.Ile1646Met | |
| ENST00000646557.1:n.105T>G | ||
| ENST00000646634.1:n.3759T>G | ||
| ENST00000646674.1:n.2196T>G | ||
| ENST00000647042.1:n.2167T>G | ||
| ENST00000647180.1:n.2057T>G | ||
| ENST00000219476.7:c.4944T>G | ENSP00000219476.3:p.Ile1648Met | |
| ENST00000350773.8:c.4875T>G | ENSP00000344383.4:p.Ile1625Met | |
| ENST00000382538.10:c.4599T>G | ENSP00000371978.6:p.Ile1533Met | |
| ENST00000401874.6:c.4743T>G | ENSP00000384468.2:p.Ile1581Met | |
| ENST00000439117.6:c.*4111T>G | ENSP00000406980.2:n.*4111T>G | |
| ENST00000439673.6:c.4635T>G | ENSP00000399232.2:p.Ile1545Met | |
| ENST00000497886.5:n.2667T>G | ||
| ENST00000568454.5:c.4776T>G | ENSP00000454487.1:p.Ile1592Met | |
| ENST00000569110.1:c.1126T>G | ||
| ENST00000569930.1:n.2059T>G | ||
| NM_000548.3:c.4944T>G , LRG_487t1:c.4944T>G | NP_000539.2:p.Ile1648Met | |
| NM_001077183.1:c.4743T>G | NP_001070651.1:p.Ile1581Met | |
| NM_001114382.1:c.4875T>G | NP_001107854.1:p.Ile1625Met | |
| XM_005255529.3:c.4815T>G | XP_005255586.2:p.Ile1605Met | |
| XM_005255531.3:c.4746T>G | XP_005255588.2:p.Ile1582Met | |
| XM_011522636.1:c.4998T>G | XP_011520938.1:p.Ile1666Met | |
| XM_011522637.1:c.4995T>G | XP_011520939.1:p.Ile1665Met | |
| XM_011522638.1:c.4887T>G | XP_011520940.1:p.Ile1629Met | |
| XM_011522639.1:c.4869T>G | XP_011520941.1:p.Ile1623Met | |
| XM_011522640.1:c.4866T>G | XP_011520942.1:p.Ile1622Met | |
| XM_011522641.1:c.4635T>G | XP_011520943.1:p.Ile1545Met | |
| NM_000548.4:c.4944T>G | NP_000539.2:p.Ile1648Met | |
| NM_001077183.2:c.4743T>G | NP_001070651.1:p.Ile1581Met | |
| NM_001114382.2:c.4875T>G | NP_001107854.1:p.Ile1625Met | |
| NM_001318827.1:c.4635T>G | NP_001305756.1:p.Ile1545Met | |
| NM_001318829.1:c.4599T>G | NP_001305758.1:p.Ile1533Met | |
| NM_001318831.1:c.4212T>G | NP_001305760.1:p.Ile1404Met | |
| NM_001318832.1:c.4776T>G | NP_001305761.1:p.Ile1592Met | |
| NM_001363528.1:c.4746T>G | NP_001350457.1:p.Ile1582Met | |
| NM_021055.2:c.4815T>G | NP_066399.2:p.Ile1605Met | |
| XM_005255531.4:c.4746T>G | XP_005255588.2:p.Ile1582Met | |
| XM_011522636.2:c.4998T>G | XP_011520938.1:p.Ile1666Met | |
| XM_011522637.2:c.4995T>G | XP_011520939.1:p.Ile1665Met | |
| XM_011522638.2:c.5160T>G | XP_011520940.2:p.Ile1720Met | |
| XM_011522639.2:c.4869T>G | XP_011520941.1:p.Ile1623Met | |
| XM_011522640.2:c.4866T>G | XP_011520942.1:p.Ile1622Met | |
| XM_017023615.1:c.4941T>G | XP_016879104.1:p.Ile1647Met | |
| XM_017023616.1:c.4812T>G | XP_016879105.1:p.Ile1604Met | |
| XM_017023617.1:c.4908T>G | XP_016879106.1:p.Ile1636Met | |
| XM_017023618.1:c.3654T>G | XP_016879107.1:p.Ile1218Met | |
| XM_024450413.1:c.4743T>G | XP_024306181.1:p.Ile1581Met | |
| NM_000548.5:c.4944T>G MANE Select | NP_000539.2:p.Ile1648Met | |
| NM_001370404.1:c.4812T>G | NP_001357333.1:p.Ile1604Met | |
| NM_001370405.1:c.4815T>G | NP_001357334.1:p.Ile1605Met | |
| NM_001077183.3:c.4743T>G | NP_001070651.1:p.Ile1581Met | |
| NM_001114382.3:c.4875T>G | NP_001107854.1:p.Ile1625Met | |
| NM_001318827.2:c.4635T>G | NP_001305756.1:p.Ile1545Met | |
| NM_001318829.2:c.4599T>G | NP_001305758.1:p.Ile1533Met | |
| NM_001318831.2:c.4212T>G | NP_001305760.1:p.Ile1404Met | |
| NM_001318832.2:c.4776T>G | NP_001305761.1:p.Ile1592Met | |
| NM_001363528.2:c.4746T>G | NP_001350457.1:p.Ile1582Met | |
| NM_021055.3:c.4815T>G | NP_066399.2:p.Ile1605Met |