Canonical Allele Identifier: CA2647250829
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707219C>A , CM000663.2:g.114707219C>A GRCh38
NC_000001.10:g.115249840C>A , CM000663.1:g.115249840C>A GRCh37
NC_000001.9:g.115051363C>A NCBI36
NG_007572.1:g.14676G>T , LRG_92:g.14676G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*875G>T MANE Select ENSP00000358548.4:n.*875G>T
ENST00000369535.4:c.*875G>T ENSP00000358548.4:n.*875G>T
NM_002524.4:c.*875G>T NP_002515.1:n.*875G>T
NM_002524.5:c.*875G>T MANE Select NP_002515.1:n.*875G>T