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.2088525C>G , CM000678.2:g.2088525C>G | GRCh38 |
| NC_000016.9:g.2138526C>G , CM000678.1:g.2138526C>G | GRCh37 |
| NC_000016.8:g.2078527C>G | NCBI36 |
| NG_005895.1:g.44220C>G , LRG_487:g.44220C>G | |
| NG_008617.1:g.54696G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3688C>G | ENSP00000455997.2:n.*3688C>G | |
| ENST00000642206.2:c.5186C>G | ENSP00000495146.2:p.Thr1729Ser | |
| ENST00000642365.2:c.5336C>G | ENSP00000495459.2:p.Thr1779Ser | |
| ENST00000644417.2:c.*5852C>G | ENSP00000493912.2:n.*5852C>G | |
| ENST00000646464.2:c.*8088C>G | ENSP00000496610.2:n.*8088C>G | |
| ENST00000219476.9:c.5339C>G MANE Select | ENSP00000219476.3:p.Thr1780Ser | |
| ENST00000350773.9:c.5270C>G | ENSP00000344383.4:p.Thr1757Ser | |
| ENST00000401874.7:c.5138C>G | ENSP00000384468.2:p.Thr1713Ser | |
| ENST00000568454.6:c.5171C>G | ENSP00000454487.1:p.Thr1724Ser | |
| ENST00000569110.2:c.1562C>G | ||
| ENST00000569930.2:n.3221C>G | ||
| ENST00000642365.1:c.3993C>G | ||
| ENST00000642561.1:c.5198C>G | ENSP00000495099.1:p.Thr1733Ser | |
| ENST00000642791.1:n.936C>G | ||
| ENST00000642797.1:c.5141C>G | ENSP00000493846.1:p.Thr1714Ser | |
| ENST00000642936.1:c.5207C>G | ENSP00000494514.1:p.Thr1736Ser | |
| ENST00000643088.1:c.5132C>G | ENSP00000494747.1:p.Thr1711Ser | |
| ENST00000643426.1:n.2987C>G | ||
| ENST00000643946.1:c.5264C>G | ENSP00000495927.1:p.Thr1755Ser | |
| ENST00000644043.1:c.5210C>G | ENSP00000496262.1:p.Thr1737Ser | |
| ENST00000644329.1:c.5225C>G | ENSP00000496611.1:p.Thr1742Ser | |
| ENST00000644335.1:c.5135C>G | ENSP00000496317.1:p.Thr1712Ser | |
| ENST00000644399.1:c.5260C>G | ||
| ENST00000645024.1:n.3423C>G | ||
| ENST00000646388.1:c.5333C>G | ENSP00000495921.1:p.Thr1778Ser | |
| ENST00000646634.1:n.4154C>G | ||
| ENST00000646674.1:n.2591C>G | ||
| ENST00000647042.1:n.2562C>G | ||
| ENST00000647180.1:n.2452C>G | ||
| ENST00000219476.7:c.5339C>G | ENSP00000219476.3:p.Thr1780Ser | |
| ENST00000350773.8:c.5270C>G | ENSP00000344383.4:p.Thr1757Ser | |
| ENST00000382538.10:c.4994C>G | ENSP00000371978.6:p.Thr1665Ser | |
| ENST00000401874.6:c.5138C>G | ENSP00000384468.2:p.Thr1713Ser | |
| ENST00000439117.6:c.*4506C>G | ENSP00000406980.2:n.*4506C>G | |
| ENST00000439673.6:c.5030C>G | ENSP00000399232.2:p.Thr1677Ser | |
| ENST00000497886.5:n.3062C>G | ||
| ENST00000568454.5:c.5171C>G | ENSP00000454487.1:p.Thr1724Ser | |
| ENST00000569110.1:c.1521C>G | ||
| ENST00000569930.1:n.2454C>G | ||
| NM_000548.3:c.5339C>G , LRG_487t1:c.5339C>G | NP_000539.2:p.Thr1780Ser | |
| NM_001077183.1:c.5138C>G | NP_001070651.1:p.Thr1713Ser | |
| NM_001114382.1:c.5270C>G | NP_001107854.1:p.Thr1757Ser | |
| XM_005255529.3:c.5210C>G | XP_005255586.2:p.Thr1737Ser | |
| XM_005255531.3:c.5141C>G | XP_005255588.2:p.Thr1714Ser | |
| XM_011522636.1:c.5393C>G | XP_011520938.1:p.Thr1798Ser | |
| XM_011522637.1:c.5390C>G | XP_011520939.1:p.Thr1797Ser | |
| XM_011522638.1:c.5282C>G | XP_011520940.1:p.Thr1761Ser | |
| XM_011522639.1:c.5264C>G | XP_011520941.1:p.Thr1755Ser | |
| XM_011522640.1:c.5261C>G | XP_011520942.1:p.Thr1754Ser | |
| XM_011522641.1:c.5030C>G | XP_011520943.1:p.Thr1677Ser | |
| NM_000548.4:c.5339C>G | NP_000539.2:p.Thr1780Ser | |
| NM_001077183.2:c.5138C>G | NP_001070651.1:p.Thr1713Ser | |
| NM_001114382.2:c.5270C>G | NP_001107854.1:p.Thr1757Ser | |
| NM_001318827.1:c.5030C>G | NP_001305756.1:p.Thr1677Ser | |
| NM_001318829.1:c.4994C>G | NP_001305758.1:p.Thr1665Ser | |
| NM_001318831.1:c.4607C>G | NP_001305760.1:p.Thr1536Ser | |
| NM_001318832.1:c.5171C>G | NP_001305761.1:p.Thr1724Ser | |
| NM_001363528.1:c.5141C>G | NP_001350457.1:p.Thr1714Ser | |
| NM_021055.2:c.5210C>G | NP_066399.2:p.Thr1737Ser | |
| XM_005255531.4:c.5141C>G | XP_005255588.2:p.Thr1714Ser | |
| XM_011522636.2:c.5393C>G | XP_011520938.1:p.Thr1798Ser | |
| XM_011522637.2:c.5390C>G | XP_011520939.1:p.Thr1797Ser | |
| XM_011522638.2:c.5555C>G | XP_011520940.2:p.Thr1852Ser | |
| XM_011522639.2:c.5264C>G | XP_011520941.1:p.Thr1755Ser | |
| XM_011522640.2:c.5261C>G | XP_011520942.1:p.Thr1754Ser | |
| XM_017023615.1:c.5336C>G | XP_016879104.1:p.Thr1779Ser | |
| XM_017023616.1:c.5207C>G | XP_016879105.1:p.Thr1736Ser | |
| XM_017023617.1:c.5303C>G | XP_016879106.1:p.Thr1768Ser | |
| XM_017023618.1:c.4049C>G | XP_016879107.1:p.Thr1350Ser | |
| XM_024450413.1:c.5225C>G | XP_024306181.1:p.Thr1742Ser | |
| NM_000548.5:c.5339C>G MANE Select | NP_000539.2:p.Thr1780Ser | |
| NM_001370404.1:c.5207C>G | NP_001357333.1:p.Thr1736Ser | |
| NM_001370405.1:c.5198C>G | NP_001357334.1:p.Thr1733Ser | |
| NM_001077183.3:c.5138C>G | NP_001070651.1:p.Thr1713Ser | |
| NM_001114382.3:c.5270C>G | NP_001107854.1:p.Thr1757Ser | |
| NM_001318827.2:c.5030C>G | NP_001305756.1:p.Thr1677Ser | |
| NM_001318829.2:c.4994C>G | NP_001305758.1:p.Thr1665Ser | |
| NM_001318831.2:c.4607C>G | NP_001305760.1:p.Thr1536Ser | |
| NM_001318832.2:c.5171C>G | NP_001305761.1:p.Thr1724Ser | |
| NM_001363528.2:c.5141C>G | NP_001350457.1:p.Thr1714Ser | |
| NM_021055.3:c.5210C>G | NP_066399.2:p.Thr1737Ser |