Canonical Allele Identifier: CA1190285431
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1658927312

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706748T>A , CM000663.2:g.114706748T>A GRCh38
NC_000001.10:g.115249369T>A , CM000663.1:g.115249369T>A GRCh37
NC_000001.9:g.115050892T>A NCBI36
NG_007572.1:g.15147A>T , LRG_92:g.15147A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1346A>T MANE Select ENSP00000358548.4:n.*1346A>T
ENST00000369535.4:c.*1346A>T ENSP00000358548.4:n.*1346A>T
NM_002524.4:c.*1346A>T NP_002515.1:n.*1346A>T
NM_002524.5:c.*1346A>T MANE Select NP_002515.1:n.*1346A>T