Canonical Allele Identifier: CA257019
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13902
dbSNP Id: rs267606921
COSMIC: COSM222543

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713941G>A , CM000663.2:g.114713941G>A GRCh38
NC_000001.10:g.115256562G>A , CM000663.1:g.115256562G>A GRCh37
NC_000001.9:g.115058085G>A NCBI36
NG_007572.1:g.7954C>T , LRG_92:g.7954C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.149C>T MANE Select ENSP00000358548.4:p.Thr50Ile
ENST00000369535.4:c.149C>T ENSP00000358548.4:p.Thr50Ile
NM_002524.4:c.149C>T NP_002515.1:p.Thr50Ile
NM_002524.5:c.149C>T MANE Select NP_002515.1:p.Thr50Ile