Revel Score:
ENST00000335295 (MANE Select)
0.502
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226578C>T , CM000673.2:g.5226578C>T | GRCh38 |
| NC_000011.9:g.5247808C>T , CM000673.1:g.5247808C>T | GRCh37 |
| NC_000011.8:g.5204384C>T | NCBI36 |
| NG_000007.3:g.71038G>A | |
| NG_059281.1:g.5494G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.314G>A | ENSP00000494175.1:p.Arg105Lys | |
| ENST00000335295.4:c.314G>A MANE Select | ENSP00000333994.3:p.Arg105Lys | |
| ENST00000475226.1:n.246G>A | ||
| ENST00000485743.1:n.365G>A | ||
| ENST00000633227.1:c.*130G>A | ENSP00000488004.1:n.*130G>A | |
| NM_000518.4:c.314G>A | NP_000509.1:p.Arg105Lys | |
| NM_000518.5:c.314G>A MANE Select | NP_000509.1:p.Arg105Lys |