WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Linked Data
gnomAD v4:
9-131518508-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131518508G>C , CM000671.2:g.131518508G>C | GRCh38 |
| NC_000009.11:g.134393895G>C , CM000671.1:g.134393895G>C | GRCh37 |
| NC_000009.10:g.133383716G>C | NCBI36 |
| NG_008896.1:g.20607G>C | |
| NG_008896.2:g.20607G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000341012.13:c.1174G>C | ENSP00000343034.7:p.Val392Leu | |
| ENST00000404875.7:n.1876G>C | ||
| ENST00000423007.6:c.1393G>C | ENSP00000404119.2:p.Val465Leu | |
| ENST00000677295.2:c.*1680G>C | ENSP00000504346.2:n.*1680G>C | |
| ENST00000678264.2:c.*1519G>C | ENSP00000503157.2:n.*1519G>C | |
| ENST00000682070.1:n.1801G>C | ||
| ENST00000682535.1:n.108G>C | ||
| ENST00000682539.1:c.274G>C | ||
| ENST00000682813.1:n.1601G>C | ||
| ENST00000683110.1:n.64G>C | ||
| ENST00000683392.1:n.4083G>C | ||
| ENST00000683712.1:n.1741G>C | ||
| ENST00000683900.1:n.3236G>C | ||
| ENST00000684062.1:n.2002G>C | ||
| ENST00000684579.1:n.3182G>C | ||
| ENST00000684679.1:n.563G>C | ||
| ENST00000341012.12:c.1174G>C | ENSP00000343034.7:p.Val392Leu | |
| ENST00000372220.5:c.205G>C | ENSP00000361294.5:p.Val69Leu | |
| ENST00000372228.9:c.1402G>C | ENSP00000361302.3:p.Val468Leu | |
| ENST00000402686.8:c.1336G>C MANE Select | ENSP00000385797.4:p.Val446Leu | |
| ENST00000676640.1:c.1336G>C | ENSP00000503281.1:p.Val446Leu | |
| ENST00000676803.1:c.511G>C | ENSP00000503093.1:p.Val171Leu | |
| ENST00000676835.1:c.*551G>C | ENSP00000502911.1:n.*551G>C | |
| ENST00000677029.1:c.880G>C | ENSP00000502936.1:p.Val294Leu | |
| ENST00000677099.1:c.*1046G>C | ENSP00000504553.1:n.*1046G>C | |
| ENST00000677216.1:c.985G>C | ENSP00000503772.1:p.Val329Leu | |
| ENST00000677221.1:n.361G>C | ||
| ENST00000677295.1:c.*713G>C | ENSP00000504346.1:n.*713G>C | |
| ENST00000677444.1:c.1142G>C | ||
| ENST00000677586.1:n.817G>C | ||
| ENST00000677626.1:c.985G>C | ENSP00000503552.1:p.Val329Leu | |
| ENST00000677677.1:n.1296G>C | ||
| ENST00000677853.1:c.*344G>C | ENSP00000503488.1:n.*344G>C | |
| ENST00000677983.1:n.425G>C | ||
| ENST00000678202.1:n.356G>C | ||
| ENST00000678264.1:c.*713G>C | ENSP00000503157.1:n.*713G>C | |
| ENST00000678303.1:c.1246G>C | ENSP00000503696.1:p.Val416Leu | |
| ENST00000678366.1:c.*1585G>C | ENSP00000504353.1:n.*1585G>C | |
| ENST00000678546.1:c.*1281G>C | ENSP00000503062.1:n.*1281G>C | |
| ENST00000678548.1:c.*1408G>C | ENSP00000503934.1:n.*1408G>C | |
| ENST00000678626.1:n.1033G>C | ||
| ENST00000678733.1:c.417G>C | ||
| ENST00000678739.1:c.*1662G>C | ENSP00000503806.1:n.*1662G>C | |
| ENST00000678795.1:n.423G>C | ||
| ENST00000678833.1:c.*783G>C | ENSP00000503893.1:n.*783G>C | |
| ENST00000678942.1:c.516G>C | ENSP00000504690.1:n.516G>C | |
| ENST00000679023.1:c.1174G>C | ENSP00000503718.1:p.Val392Leu | |
| ENST00000679076.1:c.955G>C | ||
| ENST00000679111.1:c.1336G>C | ENSP00000504257.1:p.Val446Leu | |
| ENST00000679189.1:c.985G>C | ENSP00000503356.1:p.Val329Leu | |
| ENST00000341012.11:c.1174G>C | ENSP00000343034.7:p.Val392Leu | |
| ENST00000372220.4:c.199G>C | ENSP00000361294.4:p.Val67Leu | |
| ENST00000372228.7:c.1402G>C | ENSP00000361302.3:p.Val468Leu | |
| ENST00000402686.7:c.1336G>C | ENSP00000385797.3:p.Val446Leu | |
| ENST00000404875.6:c.985G>C | ENSP00000384531.2:p.Val329Leu | |
| ENST00000423007.5:c.1336G>C | ENSP00000404119.1:p.Val446Leu | |
| ENST00000485278.5:n.1891G>C | ||
| NM_001077365.1:c.1336G>C | NP_001070833.1:p.Val446Leu | |
| NM_001077366.1:c.1174G>C | NP_001070834.1:p.Val392Leu | |
| NM_001136113.1:c.1336G>C | NP_001129585.1:p.Val446Leu | |
| NM_001136114.1:c.985G>C | NP_001129586.1:p.Val329Leu | |
| NM_007171.3:c.1402G>C | NP_009102.3:p.Val468Leu | |
| XM_005272156.1:c.1402G>C | XP_005272213.1:p.Val468Leu | |
| XM_005272158.1:c.1240G>C | XP_005272215.1:p.Val414Leu | |
| XM_005272159.1:c.1051G>C | XP_005272216.1:p.Val351Leu | |
| XM_005272162.1:c.205G>C | XP_005272219.1:p.Val69Leu | |
| XM_006716932.1:c.1051G>C | XP_006716995.1:p.Val351Leu | |
| XM_011518140.1:c.1255G>C | XP_011516442.1:p.Val419Leu | |
| XM_011518141.1:c.1189G>C | XP_011516443.1:p.Val397Leu | |
| XM_011518142.1:c.1093G>C | XP_011516444.1:p.Val365Leu | |
| XM_011518143.1:c.1087G>C | XP_011516445.1:p.Val363Leu | |
| XM_011518144.1:c.1402G>C | XP_011516446.1:p.Val468Leu | |
| XM_011518145.1:c.946G>C | XP_011516447.1:p.Val316Leu | |
| XM_011518146.1:c.1087G>C | XP_011516448.1:p.Val363Leu | |
| XM_011518147.1:c.274G>C | XP_011516449.1:p.Val92Leu | |
| XR_929703.1:n.1578G>C | ||
| NM_001353193.1:c.1402G>C | NP_001340122.1:p.Val468Leu | |
| NM_001353194.1:c.1174G>C | NP_001340123.1:p.Val392Leu | |
| NM_001353195.1:c.985G>C | NP_001340124.1:p.Val329Leu | |
| NM_001353196.1:c.1246G>C | NP_001340125.1:p.Val416Leu | |
| NM_001353197.1:c.1240G>C | NP_001340126.1:p.Val414Leu | |
| NM_001353198.1:c.1240G>C | NP_001340127.1:p.Val414Leu | |
| NM_001353199.1:c.1051G>C | NP_001340128.1:p.Val351Leu | |
| NM_001353200.1:c.880G>C | NP_001340129.1:p.Val294Leu | |
| NR_148391.1:n.1386G>C | ||
| NR_148392.1:n.1604G>C | ||
| NR_148393.1:n.1386G>C | ||
| NR_148394.1:n.1279G>C | ||
| NR_148395.1:n.1538G>C | ||
| NR_148396.1:n.1172G>C | ||
| NR_148397.1:n.1436G>C | ||
| NR_148398.1:n.1391G>C | ||
| NR_148399.1:n.1778G>C | ||
| NR_148400.1:n.1377G>C | ||
| XM_005272162.3:c.205G>C | XP_005272219.1:p.Val69Leu | |
| XM_006716932.2:c.1051G>C | XP_006716995.1:p.Val351Leu | |
| XM_011518140.2:c.1255G>C | XP_011516442.1:p.Val419Leu | |
| XM_011518141.2:c.1189G>C | XP_011516443.1:p.Val397Leu | |
| XM_011518142.2:c.1093G>C | XP_011516444.1:p.Val365Leu | |
| XM_011518143.2:c.1087G>C | XP_011516445.1:p.Val363Leu | |
| XM_011518145.2:c.946G>C | XP_011516447.1:p.Val316Leu | |
| XM_017014205.2:c.205G>C | XP_016869694.1:p.Val69Leu | |
| XM_024447380.1:c.205G>C | XP_024303148.1:p.Val69Leu | |
| XM_024447381.1:c.511G>C | XP_024303149.1:p.Val171Leu | |
| XM_024447382.1:c.205G>C | XP_024303150.1:p.Val69Leu | |
| XR_001746160.2:n.1506G>C | ||
| XR_001746162.2:n.1572G>C | ||
| XR_001746164.1:n.1289G>C | ||
| XR_001746166.2:n.1723G>C | ||
| NM_001077365.2:c.1336G>C MANE Select | NP_001070833.1:p.Val446Leu | |
| NM_001077366.2:c.1174G>C | NP_001070834.1:p.Val392Leu | |
| NM_001136113.2:c.1336G>C | NP_001129585.1:p.Val446Leu | |
| NM_001136114.2:c.985G>C | NP_001129586.1:p.Val329Leu | |
| NM_001353193.2:c.1402G>C | NP_001340122.2:p.Val468Leu | |
| NM_001353194.2:c.1174G>C | NP_001340123.1:p.Val392Leu | |
| NM_001353195.2:c.985G>C | NP_001340124.1:p.Val329Leu | |
| NM_001353196.2:c.1246G>C | NP_001340125.1:p.Val416Leu | |
| NM_001353197.2:c.1240G>C | NP_001340126.2:p.Val414Leu | |
| NM_001353198.2:c.1240G>C | NP_001340127.2:p.Val414Leu | |
| NM_001353199.2:c.1051G>C | NP_001340128.2:p.Val351Leu | |
| NM_001353200.2:c.880G>C | NP_001340129.1:p.Val294Leu | |
| NM_001374689.1:c.1324G>C | NP_001361618.1:p.Val442Leu | |
| NM_001374690.1:c.1336G>C | NP_001361619.1:p.Val446Leu | |
| NM_001374691.1:c.985G>C | NP_001361620.1:p.Val329Leu | |
| NM_001374692.1:c.985G>C | NP_001361621.1:p.Val329Leu | |
| NM_001374693.1:c.985G>C | NP_001361622.1:p.Val329Leu | |
| NM_001374695.1:c.946G>C | NP_001361624.1:p.Val316Leu | |
| NM_007171.4:c.1402G>C | NP_009102.4:p.Val468Leu | |
| NR_148391.2:n.1370G>C | ||
| NR_148392.2:n.1588G>C | ||
| NR_148393.2:n.1370G>C | ||
| NR_148394.2:n.1263G>C | ||
| NR_148395.2:n.1522G>C | ||
| NR_148396.2:n.1156G>C | ||
| NR_148397.2:n.1420G>C | ||
| NR_148398.2:n.1375G>C | ||
| NR_148399.2:n.1762G>C | ||
| NR_148400.2:n.1361G>C |