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.2088531C>A , CM000678.2:g.2088531C>A | GRCh38 |
| NC_000016.9:g.2138532C>A , CM000678.1:g.2138532C>A | GRCh37 |
| NC_000016.8:g.2078533C>A | NCBI36 |
| NG_005895.1:g.44226C>A , LRG_487:g.44226C>A | |
| NG_008617.1:g.54690G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3694C>A | ENSP00000455997.2:n.*3694C>A | |
| ENST00000642206.2:c.5192C>A | ENSP00000495146.2:p.Ala1731Asp | |
| ENST00000642365.2:c.5342C>A | ENSP00000495459.2:p.Ala1781Asp | |
| ENST00000644417.2:c.*5858C>A | ENSP00000493912.2:n.*5858C>A | |
| ENST00000646464.2:c.*8094C>A | ENSP00000496610.2:n.*8094C>A | |
| ENST00000219476.9:c.5345C>A MANE Select | ENSP00000219476.3:p.Ala1782Asp | |
| ENST00000350773.9:c.5276C>A | ENSP00000344383.4:p.Ala1759Asp | |
| ENST00000401874.7:c.5144C>A | ENSP00000384468.2:p.Ala1715Asp | |
| ENST00000568454.6:c.5177C>A | ENSP00000454487.1:p.Ala1726Asp | |
| ENST00000569110.2:c.1568C>A | ||
| ENST00000569930.2:n.3227C>A | ||
| ENST00000642365.1:c.3999C>A | ||
| ENST00000642561.1:c.5204C>A | ENSP00000495099.1:p.Ala1735Asp | |
| ENST00000642791.1:n.942C>A | ||
| ENST00000642797.1:c.5147C>A | ENSP00000493846.1:p.Ala1716Asp | |
| ENST00000642936.1:c.5213C>A | ENSP00000494514.1:p.Ala1738Asp | |
| ENST00000643088.1:c.5138C>A | ENSP00000494747.1:p.Ala1713Asp | |
| ENST00000643426.1:n.2993C>A | ||
| ENST00000643946.1:c.5270C>A | ENSP00000495927.1:p.Ala1757Asp | |
| ENST00000644043.1:c.5216C>A | ENSP00000496262.1:p.Ala1739Asp | |
| ENST00000644329.1:c.5231C>A | ENSP00000496611.1:p.Ala1744Asp | |
| ENST00000644335.1:c.5141C>A | ENSP00000496317.1:p.Ala1714Asp | |
| ENST00000644399.1:c.5266C>A | ||
| ENST00000645024.1:n.3429C>A | ||
| ENST00000646388.1:c.5339C>A | ENSP00000495921.1:p.Ala1780Asp | |
| ENST00000646634.1:n.4160C>A | ||
| ENST00000646674.1:n.2597C>A | ||
| ENST00000647042.1:n.2568C>A | ||
| ENST00000647180.1:n.2458C>A | ||
| ENST00000219476.7:c.5345C>A | ENSP00000219476.3:p.Ala1782Asp | |
| ENST00000350773.8:c.5276C>A | ENSP00000344383.4:p.Ala1759Asp | |
| ENST00000382538.10:c.5000C>A | ENSP00000371978.6:p.Ala1667Asp | |
| ENST00000401874.6:c.5144C>A | ENSP00000384468.2:p.Ala1715Asp | |
| ENST00000439117.6:c.*4512C>A | ENSP00000406980.2:n.*4512C>A | |
| ENST00000439673.6:c.5036C>A | ENSP00000399232.2:p.Ala1679Asp | |
| ENST00000497886.5:n.3068C>A | ||
| ENST00000568454.5:c.5177C>A | ENSP00000454487.1:p.Ala1726Asp | |
| ENST00000569110.1:c.1527C>A | ||
| ENST00000569930.1:n.2460C>A | ||
| NM_000548.3:c.5345C>A , LRG_487t1:c.5345C>A | NP_000539.2:p.Ala1782Asp | |
| NM_001077183.1:c.5144C>A | NP_001070651.1:p.Ala1715Asp | |
| NM_001114382.1:c.5276C>A | NP_001107854.1:p.Ala1759Asp | |
| XM_005255529.3:c.5216C>A | XP_005255586.2:p.Ala1739Asp | |
| XM_005255531.3:c.5147C>A | XP_005255588.2:p.Ala1716Asp | |
| XM_011522636.1:c.5399C>A | XP_011520938.1:p.Ala1800Asp | |
| XM_011522637.1:c.5396C>A | XP_011520939.1:p.Ala1799Asp | |
| XM_011522638.1:c.5288C>A | XP_011520940.1:p.Ala1763Asp | |
| XM_011522639.1:c.5270C>A | XP_011520941.1:p.Ala1757Asp | |
| XM_011522640.1:c.5267C>A | XP_011520942.1:p.Ala1756Asp | |
| XM_011522641.1:c.5036C>A | XP_011520943.1:p.Ala1679Asp | |
| NM_000548.4:c.5345C>A | NP_000539.2:p.Ala1782Asp | |
| NM_001077183.2:c.5144C>A | NP_001070651.1:p.Ala1715Asp | |
| NM_001114382.2:c.5276C>A | NP_001107854.1:p.Ala1759Asp | |
| NM_001318827.1:c.5036C>A | NP_001305756.1:p.Ala1679Asp | |
| NM_001318829.1:c.5000C>A | NP_001305758.1:p.Ala1667Asp | |
| NM_001318831.1:c.4613C>A | NP_001305760.1:p.Ala1538Asp | |
| NM_001318832.1:c.5177C>A | NP_001305761.1:p.Ala1726Asp | |
| NM_001363528.1:c.5147C>A | NP_001350457.1:p.Ala1716Asp | |
| NM_021055.2:c.5216C>A | NP_066399.2:p.Ala1739Asp | |
| XM_005255531.4:c.5147C>A | XP_005255588.2:p.Ala1716Asp | |
| XM_011522636.2:c.5399C>A | XP_011520938.1:p.Ala1800Asp | |
| XM_011522637.2:c.5396C>A | XP_011520939.1:p.Ala1799Asp | |
| XM_011522638.2:c.5561C>A | XP_011520940.2:p.Ala1854Asp | |
| XM_011522639.2:c.5270C>A | XP_011520941.1:p.Ala1757Asp | |
| XM_011522640.2:c.5267C>A | XP_011520942.1:p.Ala1756Asp | |
| XM_017023615.1:c.5342C>A | XP_016879104.1:p.Ala1781Asp | |
| XM_017023616.1:c.5213C>A | XP_016879105.1:p.Ala1738Asp | |
| XM_017023617.1:c.5309C>A | XP_016879106.1:p.Ala1770Asp | |
| XM_017023618.1:c.4055C>A | XP_016879107.1:p.Ala1352Asp | |
| XM_024450413.1:c.5231C>A | XP_024306181.1:p.Ala1744Asp | |
| NM_000548.5:c.5345C>A MANE Select | NP_000539.2:p.Ala1782Asp | |
| NM_001370404.1:c.5213C>A | NP_001357333.1:p.Ala1738Asp | |
| NM_001370405.1:c.5204C>A | NP_001357334.1:p.Ala1735Asp | |
| NM_001077183.3:c.5144C>A | NP_001070651.1:p.Ala1715Asp | |
| NM_001114382.3:c.5276C>A | NP_001107854.1:p.Ala1759Asp | |
| NM_001318827.2:c.5036C>A | NP_001305756.1:p.Ala1679Asp | |
| NM_001318829.2:c.5000C>A | NP_001305758.1:p.Ala1667Asp | |
| NM_001318831.2:c.4613C>A | NP_001305760.1:p.Ala1538Asp | |
| NM_001318832.2:c.5177C>A | NP_001305761.1:p.Ala1726Asp | |
| NM_001363528.2:c.5147C>A | NP_001350457.1:p.Ala1716Asp | |
| NM_021055.3:c.5216C>A | NP_066399.2:p.Ala1739Asp |