Linked Data
ClinVar Variation Id:
521109
dbSNP Id:
rs201132615
ExAC:
12:110232249 A / C
gnomAD v2:
12-110232249-A-C
gnomAD v3:
12-109794444-A-C
gnomAD v4:
12-109794444-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.109794444A>C , CM000674.2:g.109794444A>C | GRCh38 |
| NC_000012.11:g.110232249A>C , CM000674.1:g.110232249A>C | GRCh37 |
| NC_000012.10:g.108716632A>C | NCBI36 |
| NG_017090.1:g.43964T>G , LRG_372:g.43964T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261740.7:c.1376T>G MANE Select | ENSP00000261740.2:p.Leu459Arg | |
| ENST00000418703.7:c.1376T>G | ENSP00000406191.2:p.Leu459Arg | |
| ENST00000674908.1:c.*463T>G | ENSP00000502012.1:n.*463T>G | |
| ENST00000675533.1:n.1407T>G | ||
| ENST00000675670.1:c.1376T>G | ENSP00000502135.1:p.Leu459Arg | |
| ENST00000676376.1:n.1407T>G | ||
| ENST00000261740.6:c.1376T>G | ENSP00000261740.2:p.Leu459Arg | |
| ENST00000418703.6:c.1376T>G | ENSP00000406191.2:p.Leu459Arg | |
| ENST00000536838.1:c.1274T>G | ENSP00000444336.1:p.Leu425Arg | |
| ENST00000537083.5:c.1196T>G | ENSP00000442738.1:p.Leu399Arg | |
| ENST00000538125.5:c.1376T>G | ENSP00000437449.1:p.Leu459Arg | |
| ENST00000541794.5:c.1235T>G | ENSP00000442167.1:p.Leu412Arg | |
| ENST00000544971.5:c.1055T>G | ENSP00000443611.1:p.Leu352Arg | |
| NM_001177428.1:c.1235T>G | NP_001170899.1:p.Leu412Arg | |
| NM_001177431.1:c.1274T>G | NP_001170902.1:p.Leu425Arg | |
| NM_001177433.1:c.1055T>G | NP_001170904.1:p.Leu352Arg | |
| NM_021625.4:c.1376T>G , LRG_372t1:c.1376T>G | NP_067638.3:p.Leu459Arg | |
| NM_147204.2:c.1196T>G | NP_671737.1:p.Leu399Arg | |
| XM_005253918.1:c.1376T>G | XP_005253975.1:p.Leu459Arg | |
| XM_011538630.1:c.1376T>G | XP_011536932.1:p.Leu459Arg | |
| XM_011538631.1:c.1235T>G | XP_011536933.1:p.Leu412Arg | |
| XM_011538632.1:c.1196T>G | XP_011536934.1:p.Leu399Arg | |
| XM_011538633.1:c.1055T>G | XP_011536935.1:p.Leu352Arg | |
| XM_011538634.1:c.1376T>G | XP_011536936.1:p.Leu459Arg | |
| XM_011538635.1:c.1529T>G | XP_011536937.1:p.Leu510Arg | |
| XM_011538636.1:c.1529T>G | XP_011536938.1:p.Leu510Arg | |
| XM_011538630.2:c.1529T>G | XP_011536932.2:p.Leu510Arg | |
| XM_011538631.2:c.1388T>G | XP_011536933.2:p.Leu463Arg | |
| XM_011538632.2:c.1349T>G | XP_011536934.2:p.Leu450Arg | |
| XM_011538633.2:c.1208T>G | XP_011536935.2:p.Leu403Arg | |
| XM_011538634.2:c.1529T>G | XP_011536936.2:p.Leu510Arg | |
| XM_011538635.2:c.1529T>G | XP_011536937.1:p.Leu510Arg | |
| XM_017019774.1:c.1376T>G | XP_016875263.1:p.Leu459Arg | |
| NM_021625.5:c.1376T>G MANE Select | NP_067638.3:p.Leu459Arg |