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.2088290G= , CM000678.2:g.2088290G= | GRCh38 |
| NC_000016.9:g.2138291G= , CM000678.1:g.2138291G= | GRCh37 |
| NC_000016.8:g.2078292G= | NCBI36 |
| NG_005895.1:g.43985G= , LRG_487:g.43985G= | |
| NG_008617.1:g.54931C= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3573G= | ENSP00000455997.2:n.*3573G= | |
| ENST00000642206.2:c.5071G= | ENSP00000495146.2:p.Ala1691= | |
| ENST00000642365.2:c.5221G= | ENSP00000495459.2:p.Ala1741= | |
| ENST00000644417.2:c.*5737G= | ENSP00000493912.2:n.*5737G= | |
| ENST00000646464.2:c.*7973G= | ENSP00000496610.2:n.*7973G= | |
| ENST00000219476.9:c.5224G= MANE Select | ENSP00000219476.3:p.Ala1742= | |
| ENST00000350773.9:c.5155G= | ENSP00000344383.4:p.Ala1719= | |
| ENST00000401874.7:c.5023G= | ENSP00000384468.2:p.Ala1675= | |
| ENST00000568454.6:c.5056G= | ENSP00000454487.1:p.Ala1686= | |
| ENST00000569110.2:c.1447G= | ||
| ENST00000569930.2:n.3106G= | ||
| ENST00000642365.1:c.3878G= | ||
| ENST00000642561.1:c.5083G= | ENSP00000495099.1:p.Ala1695= | |
| ENST00000642791.1:n.821G= | ||
| ENST00000642797.1:c.5026G= | ENSP00000493846.1:p.Ala1676= | |
| ENST00000642936.1:c.5092G= | ENSP00000494514.1:p.Ala1698= | |
| ENST00000643088.1:c.5017G= | ENSP00000494747.1:p.Ala1673= | |
| ENST00000643426.1:n.2872G= | ||
| ENST00000643946.1:c.5149G= | ENSP00000495927.1:p.Ala1717= | |
| ENST00000644043.1:c.5095G= | ENSP00000496262.1:p.Ala1699= | |
| ENST00000644329.1:c.5110G= | ENSP00000496611.1:p.Ala1704= | |
| ENST00000644335.1:c.5020G= | ENSP00000496317.1:p.Ala1674= | |
| ENST00000644399.1:c.5145G= | ||
| ENST00000645024.1:n.3308G= | ||
| ENST00000646388.1:c.5218G= | ENSP00000495921.1:p.Ala1740= | |
| ENST00000646634.1:n.4039G= | ||
| ENST00000646674.1:n.2476G= | ||
| ENST00000647042.1:n.2447G= | ||
| ENST00000647180.1:n.2337G= | ||
| ENST00000219476.7:c.5224G= | ENSP00000219476.3:p.Ala1742= | |
| ENST00000350773.8:c.5155G= | ENSP00000344383.4:p.Ala1719= | |
| ENST00000382538.10:c.4879G= | ENSP00000371978.6:p.Ala1627= | |
| ENST00000401874.6:c.5023G= | ENSP00000384468.2:p.Ala1675= | |
| ENST00000439117.6:c.*4391G= | ENSP00000406980.2:n.*4391G= | |
| ENST00000439673.6:c.4915G= | ENSP00000399232.2:p.Ala1639= | |
| ENST00000497886.5:n.2947G= | ||
| ENST00000568454.5:c.5056G= | ENSP00000454487.1:p.Ala1686= | |
| ENST00000569110.1:c.1406G= | ||
| ENST00000569930.1:n.2339G= | ||
| NM_000548.3:c.5224G= , LRG_487t1:c.5224G= | NP_000539.2:p.Ala1742= | |
| NM_001077183.1:c.5023G= | NP_001070651.1:p.Ala1675= | |
| NM_001114382.1:c.5155G= | NP_001107854.1:p.Ala1719= | |
| XM_005255529.3:c.5095G= | XP_005255586.2:p.Ala1699= | |
| XM_005255531.3:c.5026G= | XP_005255588.2:p.Ala1676= | |
| XM_011522636.1:c.5278G= | XP_011520938.1:p.Ala1760= | |
| XM_011522637.1:c.5275G= | XP_011520939.1:p.Ala1759= | |
| XM_011522638.1:c.5167G= | XP_011520940.1:p.Ala1723= | |
| XM_011522639.1:c.5149G= | XP_011520941.1:p.Ala1717= | |
| XM_011522640.1:c.5146G= | XP_011520942.1:p.Ala1716= | |
| XM_011522641.1:c.4915G= | XP_011520943.1:p.Ala1639= | |
| NM_000548.4:c.5224G= | NP_000539.2:p.Ala1742= | |
| NM_001077183.2:c.5023G= | NP_001070651.1:p.Ala1675= | |
| NM_001114382.2:c.5155G= | NP_001107854.1:p.Ala1719= | |
| NM_001318827.1:c.4915G= | NP_001305756.1:p.Ala1639= | |
| NM_001318829.1:c.4879G= | NP_001305758.1:p.Ala1627= | |
| NM_001318831.1:c.4492G= | NP_001305760.1:p.Ala1498= | |
| NM_001318832.1:c.5056G= | NP_001305761.1:p.Ala1686= | |
| NM_001363528.1:c.5026G= | NP_001350457.1:p.Ala1676= | |
| NM_021055.2:c.5095G= | NP_066399.2:p.Ala1699= | |
| XM_005255531.4:c.5026G= | XP_005255588.2:p.Ala1676= | |
| XM_011522636.2:c.5278G= | XP_011520938.1:p.Ala1760= | |
| XM_011522637.2:c.5275G= | XP_011520939.1:p.Ala1759= | |
| XM_011522638.2:c.5440G= | XP_011520940.2:p.Ala1814= | |
| XM_011522639.2:c.5149G= | XP_011520941.1:p.Ala1717= | |
| XM_011522640.2:c.5146G= | XP_011520942.1:p.Ala1716= | |
| XM_017023615.1:c.5221G= | XP_016879104.1:p.Ala1741= | |
| XM_017023616.1:c.5092G= | XP_016879105.1:p.Ala1698= | |
| XM_017023617.1:c.5188G= | XP_016879106.1:p.Ala1730= | |
| XM_017023618.1:c.3934G= | XP_016879107.1:p.Ala1312= | |
| XM_024450413.1:c.5110G= | XP_024306181.1:p.Ala1704= | |
| NM_000548.5:c.5224G= MANE Select | NP_000539.2:p.Ala1742= | |
| NM_001370404.1:c.5092G= | NP_001357333.1:p.Ala1698= | |
| NM_001370405.1:c.5083G= | NP_001357334.1:p.Ala1695= | |
| NM_001077183.3:c.5023G= | NP_001070651.1:p.Ala1675= | |
| NM_001114382.3:c.5155G= | NP_001107854.1:p.Ala1719= | |
| NM_001318827.2:c.4915G= | NP_001305756.1:p.Ala1639= | |
| NM_001318829.2:c.4879G= | NP_001305758.1:p.Ala1627= | |
| NM_001318831.2:c.4492G= | NP_001305760.1:p.Ala1498= | |
| NM_001318832.2:c.5056G= | NP_001305761.1:p.Ala1686= | |
| NM_001363528.2:c.5026G= | NP_001350457.1:p.Ala1676= | |
| NM_021055.3:c.5095G= | NP_066399.2:p.Ala1699= |