Canonical Allele Identifier: CA134568
Gene: NRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 44575
dbSNP Id: rs376187980

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709736C>T , CM000663.2:g.114709736C>T GRCh38
NC_000001.10:g.115252357C>T , CM000663.1:g.115252357C>T GRCh37
NC_000001.9:g.115053880C>T NCBI36
NG_007572.1:g.12159G>A , LRG_92:g.12159G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-8G>A MANE Select ENSP00000358548.4:n.291-8G>A
ENST00000369535.4:c.291-8G>A ENSP00000358548.4:n.291-8G>A
NM_002524.4:c.291-8G>A NP_002515.1:n.291-8G>A
NM_002524.5:c.291-8G>A MANE Select NP_002515.1:n.291-8G>A