Linked Data
ClinVar Variation Id:
649685
ClinVar RCV Id:
RCV000804670
dbSNP Id:
rs558702741
gnomAD v4:
4-54733085-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54733085T>A , CM000666.2:g.54733085T>A | GRCh38 |
| NC_000004.11:g.55599251T>A , CM000666.1:g.55599251T>A | GRCh37 |
| NC_000004.10:g.55294008T>A | NCBI36 |
| NG_007456.1:g.80091T>A , LRG_307:g.80091T>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412167.7:c.2365T>A | ENSP00000390987.3:p.Leu789Met | |
| ENST00000685269.1:n.2455T>A | ||
| ENST00000686011.1:c.2362T>A | ENSP00000509704.1:p.Leu788Met | |
| ENST00000687109.1:c.2380T>A | ENSP00000509371.1:p.Leu794Met | |
| ENST00000687208.1:n.2789T>A | ||
| ENST00000687246.1:c.2349+1087T>A | ENSP00000509114.1:n.2349+1087T>A | |
| ENST00000687265.1:n.2535T>A | ||
| ENST00000687295.1:c.2365T>A | ENSP00000509450.1:p.Leu789Met | |
| ENST00000688060.1:n.174T>A | ||
| ENST00000688704.1:n.1389T>A | ||
| ENST00000689832.1:c.2377T>A | ENSP00000509084.1:p.Leu793Met | |
| ENST00000689994.1:c.1867T>A | ENSP00000509156.1:p.Leu623Met | |
| ENST00000690543.1:c.2368T>A | ENSP00000508831.1:p.Leu790Met | |
| ENST00000690917.1:n.2595T>A | ||
| ENST00000691361.1:n.1287T>A | ||
| ENST00000692783.1:c.2374T>A | ENSP00000508733.1:p.Leu792Met | |
| ENST00000692991.1:n.2474T>A | ||
| ENST00000288135.6:c.2377T>A MANE Select | ENSP00000288135.6:p.Leu793Met | |
| ENST00000288135.5:c.2377T>A | ENSP00000288135.5:p.Leu793Met | |
| ENST00000412167.6:c.2365T>A | ENSP00000390987.2:p.Leu789Met | |
| ENST00000512959.1:n.430T>A | ||
| NM_000222.2:c.2377T>A , LRG_307t1:c.2377T>A | NP_000213.1:p.Leu793Met | |
| NM_001093772.1:c.2365T>A | NP_001087241.1:p.Leu789Met | |
| XM_005265740.1:c.2380T>A | XP_005265797.1:p.Leu794Met | |
| XM_005265741.1:c.2377T>A | XP_005265798.1:p.Leu793Met | |
| XM_005265742.1:c.2368T>A | XP_005265799.1:p.Leu790Met | |
| XM_005265742.3:c.2368T>A | XP_005265799.1:p.Leu790Met | |
| XM_017008178.1:c.2374T>A | XP_016863667.1:p.Leu792Met | |
| XM_017008179.1:c.2365T>A | XP_016863668.1:p.Leu789Met | |
| XM_017008180.1:c.2362T>A | XP_016863669.1:p.Leu788Met | |
| NM_000222.3:c.2377T>A MANE Select | NP_000213.1:p.Leu793Met | |
| NM_001093772.2:c.2365T>A | NP_001087241.1:p.Leu789Met | |
| NM_001385284.1:c.2380T>A | NP_001372213.1:p.Leu794Met | |
| NM_001385285.1:c.2374T>A | NP_001372214.1:p.Leu792Met | |
| NM_001385286.1:c.2362T>A | NP_001372215.1:p.Leu788Met | |
| NM_001385288.1:c.2368T>A | NP_001372217.1:p.Leu790Met | |
| NM_001385290.1:c.2377T>A | NP_001372219.1:p.Leu793Met | |
| NM_001385292.1:c.2365T>A | NP_001372221.1:p.Leu789Met |