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:
rs2091128737
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2088228T>C , CM000678.2:g.2088228T>C | GRCh38 |
| NC_000016.9:g.2138229T>C , CM000678.1:g.2138229T>C | GRCh37 |
| NC_000016.8:g.2078230T>C | NCBI36 |
| NG_005895.1:g.43923T>C , LRG_487:g.43923T>C | |
| NG_008617.1:g.54993A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3511T>C | ENSP00000455997.2:n.*3511T>C | |
| ENST00000642206.2:c.5009T>C | ENSP00000495146.2:p.Met1670Thr | |
| ENST00000642365.2:c.5159T>C | ENSP00000495459.2:p.Met1720Thr | |
| ENST00000644417.2:c.*5675T>C | ENSP00000493912.2:n.*5675T>C | |
| ENST00000646464.2:c.*7911T>C | ENSP00000496610.2:n.*7911T>C | |
| ENST00000219476.9:c.5162T>C MANE Select | ENSP00000219476.3:p.Met1721Thr | |
| ENST00000350773.9:c.5093T>C | ENSP00000344383.4:p.Met1698Thr | |
| ENST00000401874.7:c.4961T>C | ENSP00000384468.2:p.Met1654Thr | |
| ENST00000568454.6:c.4994T>C | ENSP00000454487.1:p.Met1665Thr | |
| ENST00000569110.2:c.1385T>C | ||
| ENST00000569930.2:n.3044T>C | ||
| ENST00000642365.1:c.3816T>C | ||
| ENST00000642561.1:c.5032-11T>C | ENSP00000495099.1:n.5032-11T>C | |
| ENST00000642791.1:n.759T>C | ||
| ENST00000642797.1:c.4964T>C | ENSP00000493846.1:p.Met1655Thr | |
| ENST00000642936.1:c.5030T>C | ENSP00000494514.1:p.Met1677Thr | |
| ENST00000643088.1:c.4955T>C | ENSP00000494747.1:p.Met1652Thr | |
| ENST00000643426.1:n.2810T>C | ||
| ENST00000643946.1:c.5087T>C | ENSP00000495927.1:p.Met1696Thr | |
| ENST00000644043.1:c.5033T>C | ENSP00000496262.1:p.Met1678Thr | |
| ENST00000644329.1:c.5048T>C | ENSP00000496611.1:p.Met1683Thr | |
| ENST00000644335.1:c.4958T>C | ENSP00000496317.1:p.Met1653Thr | |
| ENST00000644399.1:c.5083T>C | ||
| ENST00000645024.1:n.3246T>C | ||
| ENST00000646388.1:c.5156T>C | ENSP00000495921.1:p.Met1719Thr | |
| ENST00000646634.1:n.3977T>C | ||
| ENST00000646674.1:n.2414T>C | ||
| ENST00000647042.1:n.2385T>C | ||
| ENST00000647180.1:n.2275T>C | ||
| ENST00000219476.7:c.5162T>C | ENSP00000219476.3:p.Met1721Thr | |
| ENST00000350773.8:c.5093T>C | ENSP00000344383.4:p.Met1698Thr | |
| ENST00000382538.10:c.4817T>C | ENSP00000371978.6:p.Met1606Thr | |
| ENST00000401874.6:c.4961T>C | ENSP00000384468.2:p.Met1654Thr | |
| ENST00000439117.6:c.*4329T>C | ENSP00000406980.2:n.*4329T>C | |
| ENST00000439673.6:c.4853T>C | ENSP00000399232.2:p.Met1618Thr | |
| ENST00000497886.5:n.2885T>C | ||
| ENST00000568454.5:c.4994T>C | ENSP00000454487.1:p.Met1665Thr | |
| ENST00000569110.1:c.1344T>C | ||
| ENST00000569930.1:n.2277T>C | ||
| NM_000548.3:c.5162T>C , LRG_487t1:c.5162T>C | NP_000539.2:p.Met1721Thr | |
| NM_001077183.1:c.4961T>C | NP_001070651.1:p.Met1654Thr | |
| NM_001114382.1:c.5093T>C | NP_001107854.1:p.Met1698Thr | |
| XM_005255529.3:c.5033T>C | XP_005255586.2:p.Met1678Thr | |
| XM_005255531.3:c.4964T>C | XP_005255588.2:p.Met1655Thr | |
| XM_011522636.1:c.5216T>C | XP_011520938.1:p.Met1739Thr | |
| XM_011522637.1:c.5213T>C | XP_011520939.1:p.Met1738Thr | |
| XM_011522638.1:c.5105T>C | XP_011520940.1:p.Met1702Thr | |
| XM_011522639.1:c.5087T>C | XP_011520941.1:p.Met1696Thr | |
| XM_011522640.1:c.5084T>C | XP_011520942.1:p.Met1695Thr | |
| XM_011522641.1:c.4853T>C | XP_011520943.1:p.Met1618Thr | |
| NM_000548.4:c.5162T>C | NP_000539.2:p.Met1721Thr | |
| NM_001077183.2:c.4961T>C | NP_001070651.1:p.Met1654Thr | |
| NM_001114382.2:c.5093T>C | NP_001107854.1:p.Met1698Thr | |
| NM_001318827.1:c.4853T>C | NP_001305756.1:p.Met1618Thr | |
| NM_001318829.1:c.4817T>C | NP_001305758.1:p.Met1606Thr | |
| NM_001318831.1:c.4430T>C | NP_001305760.1:p.Met1477Thr | |
| NM_001318832.1:c.4994T>C | NP_001305761.1:p.Met1665Thr | |
| NM_001363528.1:c.4964T>C | NP_001350457.1:p.Met1655Thr | |
| NM_021055.2:c.5033T>C | NP_066399.2:p.Met1678Thr | |
| XM_005255531.4:c.4964T>C | XP_005255588.2:p.Met1655Thr | |
| XM_011522636.2:c.5216T>C | XP_011520938.1:p.Met1739Thr | |
| XM_011522637.2:c.5213T>C | XP_011520939.1:p.Met1738Thr | |
| XM_011522638.2:c.5378T>C | XP_011520940.2:p.Met1793Thr | |
| XM_011522639.2:c.5087T>C | XP_011520941.1:p.Met1696Thr | |
| XM_011522640.2:c.5084T>C | XP_011520942.1:p.Met1695Thr | |
| XM_017023615.1:c.5159T>C | XP_016879104.1:p.Met1720Thr | |
| XM_017023616.1:c.5030T>C | XP_016879105.1:p.Met1677Thr | |
| XM_017023617.1:c.5126T>C | XP_016879106.1:p.Met1709Thr | |
| XM_017023618.1:c.3872T>C | XP_016879107.1:p.Met1291Thr | |
| XM_024450413.1:c.5048T>C | XP_024306181.1:p.Met1683Thr | |
| NM_000548.5:c.5162T>C MANE Select | NP_000539.2:p.Met1721Thr | |
| NM_001370404.1:c.5030T>C | NP_001357333.1:p.Met1677Thr | |
| NM_001370405.1:c.5032-11T>C | NP_001357334.1:n.5032-11T>C | |
| NM_001077183.3:c.4961T>C | NP_001070651.1:p.Met1654Thr | |
| NM_001114382.3:c.5093T>C | NP_001107854.1:p.Met1698Thr | |
| NM_001318827.2:c.4853T>C | NP_001305756.1:p.Met1618Thr | |
| NM_001318829.2:c.4817T>C | NP_001305758.1:p.Met1606Thr | |
| NM_001318831.2:c.4430T>C | NP_001305760.1:p.Met1477Thr | |
| NM_001318832.2:c.4994T>C | NP_001305761.1:p.Met1665Thr | |
| NM_001363528.2:c.4964T>C | NP_001350457.1:p.Met1655Thr | |
| NM_021055.3:c.5033T>C | NP_066399.2:p.Met1678Thr |