Canonical Allele Identifier: CA2647250828
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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