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.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2088249G>A , CM000678.2:g.2088249G>A | GRCh38 |
| NC_000016.9:g.2138250G>A , CM000678.1:g.2138250G>A | GRCh37 |
| NC_000016.8:g.2078251G>A | NCBI36 |
| NG_005895.1:g.43944G>A , LRG_487:g.43944G>A | |
| NG_008617.1:g.54972C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3532G>A | ENSP00000455997.2:n.*3532G>A | |
| ENST00000642206.2:c.5030G>A | ENSP00000495146.2:p.Ser1677Asn | |
| ENST00000642365.2:c.5180G>A | ENSP00000495459.2:p.Ser1727Asn | |
| ENST00000644417.2:c.*5696G>A | ENSP00000493912.2:n.*5696G>A | |
| ENST00000646464.2:c.*7932G>A | ENSP00000496610.2:n.*7932G>A | |
| ENST00000219476.9:c.5183G>A MANE Select | ENSP00000219476.3:p.Ser1728Asn | |
| ENST00000350773.9:c.5114G>A | ENSP00000344383.4:p.Ser1705Asn | |
| ENST00000401874.7:c.4982G>A | ENSP00000384468.2:p.Ser1661Asn | |
| ENST00000568454.6:c.5015G>A | ENSP00000454487.1:p.Ser1672Asn | |
| ENST00000569110.2:c.1406G>A | ||
| ENST00000569930.2:n.3065G>A | ||
| ENST00000642365.1:c.3837G>A | ||
| ENST00000642561.1:c.5042G>A | ENSP00000495099.1:p.Ser1681Asn | |
| ENST00000642791.1:n.780G>A | ||
| ENST00000642797.1:c.4985G>A | ENSP00000493846.1:p.Ser1662Asn | |
| ENST00000642936.1:c.5051G>A | ENSP00000494514.1:p.Ser1684Asn | |
| ENST00000643088.1:c.4976G>A | ENSP00000494747.1:p.Ser1659Asn | |
| ENST00000643426.1:n.2831G>A | ||
| ENST00000643946.1:c.5108G>A | ENSP00000495927.1:p.Ser1703Asn | |
| ENST00000644043.1:c.5054G>A | ENSP00000496262.1:p.Ser1685Asn | |
| ENST00000644329.1:c.5069G>A | ENSP00000496611.1:p.Ser1690Asn | |
| ENST00000644335.1:c.4979G>A | ENSP00000496317.1:p.Ser1660Asn | |
| ENST00000644399.1:c.5104G>A | ||
| ENST00000645024.1:n.3267G>A | ||
| ENST00000646388.1:c.5177G>A | ENSP00000495921.1:p.Ser1726Asn | |
| ENST00000646634.1:n.3998G>A | ||
| ENST00000646674.1:n.2435G>A | ||
| ENST00000647042.1:n.2406G>A | ||
| ENST00000647180.1:n.2296G>A | ||
| ENST00000219476.7:c.5183G>A | ENSP00000219476.3:p.Ser1728Asn | |
| ENST00000350773.8:c.5114G>A | ENSP00000344383.4:p.Ser1705Asn | |
| ENST00000382538.10:c.4838G>A | ENSP00000371978.6:p.Ser1613Asn | |
| ENST00000401874.6:c.4982G>A | ENSP00000384468.2:p.Ser1661Asn | |
| ENST00000439117.6:c.*4350G>A | ENSP00000406980.2:n.*4350G>A | |
| ENST00000439673.6:c.4874G>A | ENSP00000399232.2:p.Ser1625Asn | |
| ENST00000497886.5:n.2906G>A | ||
| ENST00000568454.5:c.5015G>A | ENSP00000454487.1:p.Ser1672Asn | |
| ENST00000569110.1:c.1365G>A | ||
| ENST00000569930.1:n.2298G>A | ||
| NM_000548.3:c.5183G>A , LRG_487t1:c.5183G>A | NP_000539.2:p.Ser1728Asn | |
| NM_001077183.1:c.4982G>A | NP_001070651.1:p.Ser1661Asn | |
| NM_001114382.1:c.5114G>A | NP_001107854.1:p.Ser1705Asn | |
| XM_005255529.3:c.5054G>A | XP_005255586.2:p.Ser1685Asn | |
| XM_005255531.3:c.4985G>A | XP_005255588.2:p.Ser1662Asn | |
| XM_011522636.1:c.5237G>A | XP_011520938.1:p.Ser1746Asn | |
| XM_011522637.1:c.5234G>A | XP_011520939.1:p.Ser1745Asn | |
| XM_011522638.1:c.5126G>A | XP_011520940.1:p.Ser1709Asn | |
| XM_011522639.1:c.5108G>A | XP_011520941.1:p.Ser1703Asn | |
| XM_011522640.1:c.5105G>A | XP_011520942.1:p.Ser1702Asn | |
| XM_011522641.1:c.4874G>A | XP_011520943.1:p.Ser1625Asn | |
| NM_000548.4:c.5183G>A | NP_000539.2:p.Ser1728Asn | |
| NM_001077183.2:c.4982G>A | NP_001070651.1:p.Ser1661Asn | |
| NM_001114382.2:c.5114G>A | NP_001107854.1:p.Ser1705Asn | |
| NM_001318827.1:c.4874G>A | NP_001305756.1:p.Ser1625Asn | |
| NM_001318829.1:c.4838G>A | NP_001305758.1:p.Ser1613Asn | |
| NM_001318831.1:c.4451G>A | NP_001305760.1:p.Ser1484Asn | |
| NM_001318832.1:c.5015G>A | NP_001305761.1:p.Ser1672Asn | |
| NM_001363528.1:c.4985G>A | NP_001350457.1:p.Ser1662Asn | |
| NM_021055.2:c.5054G>A | NP_066399.2:p.Ser1685Asn | |
| XM_005255531.4:c.4985G>A | XP_005255588.2:p.Ser1662Asn | |
| XM_011522636.2:c.5237G>A | XP_011520938.1:p.Ser1746Asn | |
| XM_011522637.2:c.5234G>A | XP_011520939.1:p.Ser1745Asn | |
| XM_011522638.2:c.5399G>A | XP_011520940.2:p.Ser1800Asn | |
| XM_011522639.2:c.5108G>A | XP_011520941.1:p.Ser1703Asn | |
| XM_011522640.2:c.5105G>A | XP_011520942.1:p.Ser1702Asn | |
| XM_017023615.1:c.5180G>A | XP_016879104.1:p.Ser1727Asn | |
| XM_017023616.1:c.5051G>A | XP_016879105.1:p.Ser1684Asn | |
| XM_017023617.1:c.5147G>A | XP_016879106.1:p.Ser1716Asn | |
| XM_017023618.1:c.3893G>A | XP_016879107.1:p.Ser1298Asn | |
| XM_024450413.1:c.5069G>A | XP_024306181.1:p.Ser1690Asn | |
| NM_000548.5:c.5183G>A MANE Select | NP_000539.2:p.Ser1728Asn | |
| NM_001370404.1:c.5051G>A | NP_001357333.1:p.Ser1684Asn | |
| NM_001370405.1:c.5042G>A | NP_001357334.1:p.Ser1681Asn | |
| NM_001077183.3:c.4982G>A | NP_001070651.1:p.Ser1661Asn | |
| NM_001114382.3:c.5114G>A | NP_001107854.1:p.Ser1705Asn | |
| NM_001318827.2:c.4874G>A | NP_001305756.1:p.Ser1625Asn | |
| NM_001318829.2:c.4838G>A | NP_001305758.1:p.Ser1613Asn | |
| NM_001318831.2:c.4451G>A | NP_001305760.1:p.Ser1484Asn | |
| NM_001318832.2:c.5015G>A | NP_001305761.1:p.Ser1672Asn | |
| NM_001363528.2:c.4985G>A | NP_001350457.1:p.Ser1662Asn | |
| NM_021055.3:c.5054G>A | NP_066399.2:p.Ser1685Asn |