Linked Data
ClinVar Variation Id:
1037658
ClinVar RCV Id:
RCV001340847
dbSNP Id:
rs1722352667
gnomAD v4:
4-54728045-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54728045G>A , CM000666.2:g.54728045G>A | GRCh38 |
| NC_000004.11:g.55594211G>A , CM000666.1:g.55594211G>A | GRCh37 |
| NC_000004.10:g.55288968G>A | NCBI36 |
| NG_007456.1:g.75051G>A , LRG_307:g.75051G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412167.7:c.1905G>A | ENSP00000390987.3:p.Met635Ile | |
| ENST00000685269.1:n.1992G>A | ||
| ENST00000686011.1:c.1902G>A | ENSP00000509704.1:p.Met634Ile | |
| ENST00000687109.1:c.1917G>A | ENSP00000509371.1:p.Met639Ile | |
| ENST00000687208.1:n.2329G>A | ||
| ENST00000687246.1:c.1902G>A | ENSP00000509114.1:p.Met634Ile | |
| ENST00000687265.1:n.2072G>A | ||
| ENST00000687295.1:c.1902G>A | ENSP00000509450.1:p.Met634Ile | |
| ENST00000689832.1:c.1917G>A | ENSP00000509084.1:p.Met639Ile | |
| ENST00000689994.1:c.1404G>A | ENSP00000509156.1:p.Met468Ile | |
| ENST00000690543.1:c.1905G>A | ENSP00000508831.1:p.Met635Ile | |
| ENST00000690917.1:n.2132G>A | ||
| ENST00000691361.1:n.824G>A | ||
| ENST00000692783.1:c.1914G>A | ENSP00000508733.1:p.Met638Ile | |
| ENST00000692991.1:n.2011G>A | ||
| ENST00000288135.6:c.1914G>A MANE Select | ENSP00000288135.6:p.Met638Ile | |
| ENST00000288135.5:c.1914G>A | ENSP00000288135.5:p.Met638Ile | |
| ENST00000412167.6:c.1902G>A | ENSP00000390987.2:p.Met634Ile | |
| NM_000222.2:c.1914G>A , LRG_307t1:c.1914G>A | NP_000213.1:p.Met638Ile | |
| NM_001093772.1:c.1902G>A | NP_001087241.1:p.Met634Ile | |
| XM_005265740.1:c.1917G>A | XP_005265797.1:p.Met639Ile | |
| XM_005265741.1:c.1917G>A | XP_005265798.1:p.Met639Ile | |
| XM_005265742.1:c.1905G>A | XP_005265799.1:p.Met635Ile | |
| XM_005265742.3:c.1905G>A | XP_005265799.1:p.Met635Ile | |
| XM_017008178.1:c.1914G>A | XP_016863667.1:p.Met638Ile | |
| XM_017008179.1:c.1905G>A | XP_016863668.1:p.Met635Ile | |
| XM_017008180.1:c.1902G>A | XP_016863669.1:p.Met634Ile | |
| NM_000222.3:c.1914G>A MANE Select | NP_000213.1:p.Met638Ile | |
| NM_001093772.2:c.1902G>A | NP_001087241.1:p.Met634Ile | |
| NM_001385284.1:c.1917G>A | NP_001372213.1:p.Met639Ile | |
| NM_001385285.1:c.1914G>A | NP_001372214.1:p.Met638Ile | |
| NM_001385286.1:c.1902G>A | NP_001372215.1:p.Met634Ile | |
| NM_001385288.1:c.1905G>A | NP_001372217.1:p.Met635Ile | |
| NM_001385290.1:c.1917G>A | NP_001372219.1:p.Met639Ile | |
| NM_001385292.1:c.1905G>A | NP_001372221.1:p.Met635Ile |