Revel Score:
ENST00000335295 (MANE Select)
0.859
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225675A>C , CM000673.2:g.5225675A>C | GRCh38 |
| NC_000011.9:g.5246905A>C , CM000673.1:g.5246905A>C | GRCh37 |
| NC_000011.8:g.5203481A>C | NCBI36 |
| NG_000007.3:g.71941T>G | |
| NG_059281.1:g.6397T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.367T>G | ENSP00000494175.1:p.Phe123Val | |
| ENST00000335295.4:c.367T>G MANE Select | ENSP00000333994.3:p.Phe123Val | |
| ENST00000475226.1:n.299T>G | ||
| ENST00000633227.1:c.*183T>G | ENSP00000488004.1:n.*183T>G | |
| NM_000518.4:c.367T>G | NP_000509.1:p.Phe123Val | |
| NM_000518.5:c.367T>G MANE Select | NP_000509.1:p.Phe123Val |