Linked Data
ClinVar Variation Id:
1160050
ClinVar RCV Id:
RCV001503990
dbSNP Id:
rs2109801101
MyVariant Identifiers:
chr4:g.55599253G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54733087G>A , CM000666.2:g.54733087G>A | GRCh38 |
| NC_000004.11:g.55599253G>A , CM000666.1:g.55599253G>A | GRCh37 |
| NC_000004.10:g.55294010G>A | NCBI36 |
| NG_007456.1:g.80093G>A , LRG_307:g.80093G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412167.7:c.2367G>A | ENSP00000390987.3:p.Leu789= | |
| ENST00000685269.1:n.2457G>A | ||
| ENST00000686011.1:c.2364G>A | ENSP00000509704.1:p.Leu788= | |
| ENST00000687109.1:c.2382G>A | ENSP00000509371.1:p.Leu794= | |
| ENST00000687208.1:n.2791G>A | ||
| ENST00000687246.1:c.2349+1089G>A | ENSP00000509114.1:n.2349+1089G>A | |
| ENST00000687265.1:n.2537G>A | ||
| ENST00000687295.1:c.2367G>A | ENSP00000509450.1:p.Leu789= | |
| ENST00000688060.1:n.176G>A | ||
| ENST00000688704.1:n.1391G>A | ||
| ENST00000689832.1:c.2379G>A | ENSP00000509084.1:p.Leu793= | |
| ENST00000689994.1:c.1869G>A | ENSP00000509156.1:p.Leu623= | |
| ENST00000690543.1:c.2370G>A | ENSP00000508831.1:p.Leu790= | |
| ENST00000690917.1:n.2597G>A | ||
| ENST00000691361.1:n.1289G>A | ||
| ENST00000692783.1:c.2376G>A | ENSP00000508733.1:p.Leu792= | |
| ENST00000692991.1:n.2476G>A | ||
| ENST00000288135.6:c.2379G>A MANE Select | ENSP00000288135.6:p.Leu793= | |
| ENST00000288135.5:c.2379G>A | ENSP00000288135.5:p.Leu793= | |
| ENST00000412167.6:c.2367G>A | ENSP00000390987.2:p.Leu789= | |
| ENST00000512959.1:n.432G>A | ||
| NM_000222.2:c.2379G>A , LRG_307t1:c.2379G>A | NP_000213.1:p.Leu793= | |
| NM_001093772.1:c.2367G>A | NP_001087241.1:p.Leu789= | |
| XM_005265740.1:c.2382G>A | XP_005265797.1:p.Leu794= | |
| XM_005265741.1:c.2379G>A | XP_005265798.1:p.Leu793= | |
| XM_005265742.1:c.2370G>A | XP_005265799.1:p.Leu790= | |
| XM_005265742.3:c.2370G>A | XP_005265799.1:p.Leu790= | |
| XM_017008178.1:c.2376G>A | XP_016863667.1:p.Leu792= | |
| XM_017008179.1:c.2367G>A | XP_016863668.1:p.Leu789= | |
| XM_017008180.1:c.2364G>A | XP_016863669.1:p.Leu788= | |
| NM_000222.3:c.2379G>A MANE Select | NP_000213.1:p.Leu793= | |
| NM_001093772.2:c.2367G>A | NP_001087241.1:p.Leu789= | |
| NM_001385284.1:c.2382G>A | NP_001372213.1:p.Leu794= | |
| NM_001385285.1:c.2376G>A | NP_001372214.1:p.Leu792= | |
| NM_001385286.1:c.2364G>A | NP_001372215.1:p.Leu788= | |
| NM_001385288.1:c.2370G>A | NP_001372217.1:p.Leu790= | |
| NM_001385290.1:c.2379G>A | NP_001372219.1:p.Leu793= | |
| NM_001385292.1:c.2367G>A | NP_001372221.1:p.Leu789= |