Canonical Allele Identifier: CA123620
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 13901
dbSNP Id: rs121434596
COSMIC: COSM573
CIViC: CA123620

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716123C>T , CM000663.2:g.114716123C>T GRCh38
NC_000001.10:g.115258744C>T , CM000663.1:g.115258744C>T GRCh37
NC_000001.9:g.115060267C>T NCBI36
NG_007572.1:g.5772G>A , LRG_92:g.5772G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.38G>A MANE Select ENSP00000358548.4:p.Gly13Asp
ENST00000369535.4:c.38G>A ENSP00000358548.4:p.Gly13Asp
NM_002524.4:c.38G>A NP_002515.1:p.Gly13Asp
NM_002524.5:c.38G>A MANE Select NP_002515.1:p.Gly13Asp