Revel Score:
ENST00000278616
0.175
ENST00000452508
0.175
gnomAD v2:
gnomAD v3:
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108293340A>G , CM000673.2:g.108293340A>G | GRCh38 |
| NC_000011.9:g.108164067A>G , CM000673.1:g.108164067A>G | GRCh37 |
| NC_000011.8:g.107669277A>G | NCBI36 |
| NG_009830.1:g.75509A>G , LRG_135:g.75509A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.4639A>G | ENSP00000388058.2:p.Ile1547Val | |
| ENST00000713593.1:c.*4110A>G | ENSP00000518889.1:n.*4110A>G | |
| ENST00000278616.9:c.4639A>G | ENSP00000278616.4:p.Ile1547Val | |
| ENST00000683174.1:n.4789A>G | ||
| ENST00000527805.6:c.4611+547A>G | ENSP00000435747.2:n.4611+547A>G | |
| ENST00000675595.1:c.4474A>G | ENSP00000502563.1:p.Ile1492Val | |
| ENST00000675843.1:c.4639A>G MANE Select | ENSP00000501606.1:p.Ile1547Val | |
| ENST00000278616.8:c.4639A>G | ENSP00000278616.4:p.Ile1547Val | |
| ENST00000452508.6:c.4639A>G | ENSP00000388058.2:p.Ile1547Val | |
| ENST00000524792.5:n.854A>G | ||
| ENST00000531525.2:c.444-1587A>G | ENSP00000434327.2:n.444-1587A>G | |
| NM_000051.3:c.4639A>G , LRG_135t1:c.4639A>G | NP_000042.3:p.Ile1547Val | |
| XM_005271561.3:c.4639A>G | XP_005271618.2:p.Ile1547Val | |
| XM_005271562.3:c.4639A>G | XP_005271619.2:p.Ile1547Val | |
| XM_006718843.2:c.4639A>G | XP_006718906.1:p.Ile1547Val | |
| XM_006718845.1:c.595A>G | XP_006718908.1:p.Ile199Val | |
| XM_011542840.1:c.4639A>G | XP_011541142.1:p.Ile1547Val | |
| XM_011542841.1:c.4639A>G | XP_011541143.1:p.Ile1547Val | |
| XM_011542842.1:c.4474A>G | XP_011541144.1:p.Ile1492Val | |
| XM_011542843.1:c.4639A>G | XP_011541145.1:p.Ile1547Val | |
| XM_011542844.1:c.3595A>G | XP_011541146.1:p.Ile1199Val | |
| XM_011542845.1:c.3331A>G | XP_011541147.1:p.Ile1111Val | |
| XM_011542846.1:c.4639A>G | XP_011541148.1:p.Ile1547Val | |
| NM_001351834.1:c.4639A>G | NP_001338763.1:p.Ile1547Val | |
| XM_005271562.5:c.4639A>G | XP_005271619.2:p.Ile1547Val | |
| XM_006718843.4:c.4639A>G | XP_006718906.1:p.Ile1547Val | |
| XM_006718845.2:c.595A>G | XP_006718908.1:p.Ile199Val | |
| XM_011542840.3:c.4639A>G | XP_011541142.1:p.Ile1547Val | |
| XM_011542842.3:c.4474A>G | XP_011541144.1:p.Ile1492Val | |
| XM_011542843.2:c.4639A>G | XP_011541145.1:p.Ile1547Val | |
| XM_011542844.3:c.3595A>G | XP_011541146.1:p.Ile1199Val | |
| XM_011542845.2:c.3331A>G | XP_011541147.1:p.Ile1111Val | |
| XM_017017789.2:c.4639A>G | XP_016873278.1:p.Ile1547Val | |
| XM_017017790.2:c.4639A>G | XP_016873279.1:p.Ile1547Val | |
| XM_017017791.1:c.4639A>G | XP_016873280.1:p.Ile1547Val | |
| XM_017017792.2:c.4639A>G | XP_016873281.1:p.Ile1547Val | |
| XR_002957150.1:n.5372A>G | ||
| NM_001351834.2:c.4639A>G | NP_001338763.1:p.Ile1547Val | |
| NM_000051.4:c.4639A>G MANE Select | NP_000042.3:p.Ile1547Val |