Canonical Allele Identifier: CA1146627238
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709784A= , CM000663.2:g.114709784A= GRCh38
NC_000001.10:g.115252405A= , CM000663.1:g.115252405A= GRCh37
NC_000001.9:g.115053928A= NCBI36
NG_007572.1:g.12111T= , LRG_92:g.12111T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-56T= MANE Select ENSP00000358548.4:n.291-56T=
ENST00000369535.4:c.291-56T= ENSP00000358548.4:n.291-56T=
NM_002524.4:c.291-56T= NP_002515.1:n.291-56T=
NM_002524.5:c.291-56T= MANE Select NP_002515.1:n.291-56T=