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
dbSNP Id:
rs767191593
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2088247T>A , CM000678.2:g.2088247T>A | GRCh38 |
| NC_000016.9:g.2138248T>A , CM000678.1:g.2138248T>A | GRCh37 |
| NC_000016.8:g.2078249T>A | NCBI36 |
| NG_005895.1:g.43942T>A , LRG_487:g.43942T>A | |
| NG_008617.1:g.54974A>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3530T>A | ENSP00000455997.2:n.*3530T>A | |
| ENST00000642206.2:c.5028T>A | ENSP00000495146.2:p.His1676Gln | |
| ENST00000642365.2:c.5178T>A | ENSP00000495459.2:p.His1726Gln | |
| ENST00000644417.2:c.*5694T>A | ENSP00000493912.2:n.*5694T>A | |
| ENST00000646464.2:c.*7930T>A | ENSP00000496610.2:n.*7930T>A | |
| ENST00000219476.9:c.5181T>A MANE Select | ENSP00000219476.3:p.His1727Gln | |
| ENST00000350773.9:c.5112T>A | ENSP00000344383.4:p.His1704Gln | |
| ENST00000401874.7:c.4980T>A | ENSP00000384468.2:p.His1660Gln | |
| ENST00000568454.6:c.5013T>A | ENSP00000454487.1:p.His1671Gln | |
| ENST00000569110.2:c.1404T>A | ||
| ENST00000569930.2:n.3063T>A | ||
| ENST00000642365.1:c.3835T>A | ||
| ENST00000642561.1:c.5040T>A | ENSP00000495099.1:p.His1680Gln | |
| ENST00000642791.1:n.778T>A | ||
| ENST00000642797.1:c.4983T>A | ENSP00000493846.1:p.His1661Gln | |
| ENST00000642936.1:c.5049T>A | ENSP00000494514.1:p.His1683Gln | |
| ENST00000643088.1:c.4974T>A | ENSP00000494747.1:p.His1658Gln | |
| ENST00000643426.1:n.2829T>A | ||
| ENST00000643946.1:c.5106T>A | ENSP00000495927.1:p.His1702Gln | |
| ENST00000644043.1:c.5052T>A | ENSP00000496262.1:p.His1684Gln | |
| ENST00000644329.1:c.5067T>A | ENSP00000496611.1:p.His1689Gln | |
| ENST00000644335.1:c.4977T>A | ENSP00000496317.1:p.His1659Gln | |
| ENST00000644399.1:c.5102T>A | ||
| ENST00000645024.1:n.3265T>A | ||
| ENST00000646388.1:c.5175T>A | ENSP00000495921.1:p.His1725Gln | |
| ENST00000646634.1:n.3996T>A | ||
| ENST00000646674.1:n.2433T>A | ||
| ENST00000647042.1:n.2404T>A | ||
| ENST00000647180.1:n.2294T>A | ||
| ENST00000219476.7:c.5181T>A | ENSP00000219476.3:p.His1727Gln | |
| ENST00000350773.8:c.5112T>A | ENSP00000344383.4:p.His1704Gln | |
| ENST00000382538.10:c.4836T>A | ENSP00000371978.6:p.His1612Gln | |
| ENST00000401874.6:c.4980T>A | ENSP00000384468.2:p.His1660Gln | |
| ENST00000439117.6:c.*4348T>A | ENSP00000406980.2:n.*4348T>A | |
| ENST00000439673.6:c.4872T>A | ENSP00000399232.2:p.His1624Gln | |
| ENST00000497886.5:n.2904T>A | ||
| ENST00000568454.5:c.5013T>A | ENSP00000454487.1:p.His1671Gln | |
| ENST00000569110.1:c.1363T>A | ||
| ENST00000569930.1:n.2296T>A | ||
| NM_000548.3:c.5181T>A , LRG_487t1:c.5181T>A | NP_000539.2:p.His1727Gln | |
| NM_001077183.1:c.4980T>A | NP_001070651.1:p.His1660Gln | |
| NM_001114382.1:c.5112T>A | NP_001107854.1:p.His1704Gln | |
| XM_005255529.3:c.5052T>A | XP_005255586.2:p.His1684Gln | |
| XM_005255531.3:c.4983T>A | XP_005255588.2:p.His1661Gln | |
| XM_011522636.1:c.5235T>A | XP_011520938.1:p.His1745Gln | |
| XM_011522637.1:c.5232T>A | XP_011520939.1:p.His1744Gln | |
| XM_011522638.1:c.5124T>A | XP_011520940.1:p.His1708Gln | |
| XM_011522639.1:c.5106T>A | XP_011520941.1:p.His1702Gln | |
| XM_011522640.1:c.5103T>A | XP_011520942.1:p.His1701Gln | |
| XM_011522641.1:c.4872T>A | XP_011520943.1:p.His1624Gln | |
| NM_000548.4:c.5181T>A | NP_000539.2:p.His1727Gln | |
| NM_001077183.2:c.4980T>A | NP_001070651.1:p.His1660Gln | |
| NM_001114382.2:c.5112T>A | NP_001107854.1:p.His1704Gln | |
| NM_001318827.1:c.4872T>A | NP_001305756.1:p.His1624Gln | |
| NM_001318829.1:c.4836T>A | NP_001305758.1:p.His1612Gln | |
| NM_001318831.1:c.4449T>A | NP_001305760.1:p.His1483Gln | |
| NM_001318832.1:c.5013T>A | NP_001305761.1:p.His1671Gln | |
| NM_001363528.1:c.4983T>A | NP_001350457.1:p.His1661Gln | |
| NM_021055.2:c.5052T>A | NP_066399.2:p.His1684Gln | |
| XM_005255531.4:c.4983T>A | XP_005255588.2:p.His1661Gln | |
| XM_011522636.2:c.5235T>A | XP_011520938.1:p.His1745Gln | |
| XM_011522637.2:c.5232T>A | XP_011520939.1:p.His1744Gln | |
| XM_011522638.2:c.5397T>A | XP_011520940.2:p.His1799Gln | |
| XM_011522639.2:c.5106T>A | XP_011520941.1:p.His1702Gln | |
| XM_011522640.2:c.5103T>A | XP_011520942.1:p.His1701Gln | |
| XM_017023615.1:c.5178T>A | XP_016879104.1:p.His1726Gln | |
| XM_017023616.1:c.5049T>A | XP_016879105.1:p.His1683Gln | |
| XM_017023617.1:c.5145T>A | XP_016879106.1:p.His1715Gln | |
| XM_017023618.1:c.3891T>A | XP_016879107.1:p.His1297Gln | |
| XM_024450413.1:c.5067T>A | XP_024306181.1:p.His1689Gln | |
| NM_000548.5:c.5181T>A MANE Select | NP_000539.2:p.His1727Gln | |
| NM_001370404.1:c.5049T>A | NP_001357333.1:p.His1683Gln | |
| NM_001370405.1:c.5040T>A | NP_001357334.1:p.His1680Gln | |
| NM_001077183.3:c.4980T>A | NP_001070651.1:p.His1660Gln | |
| NM_001114382.3:c.5112T>A | NP_001107854.1:p.His1704Gln | |
| NM_001318827.2:c.4872T>A | NP_001305756.1:p.His1624Gln | |
| NM_001318829.2:c.4836T>A | NP_001305758.1:p.His1612Gln | |
| NM_001318831.2:c.4449T>A | NP_001305760.1:p.His1483Gln | |
| NM_001318832.2:c.5013T>A | NP_001305761.1:p.His1671Gln | |
| NM_001363528.2:c.4983T>A | NP_001350457.1:p.His1661Gln | |
| NM_021055.3:c.5052T>A | NP_066399.2:p.His1684Gln |