Canonical Allele Identifier: CA1142050500

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705427A= , CM000663.2:g.114705427A=	GRCh38
NC_000001.10:g.115248048A= , CM000663.1:g.115248048A=	GRCh37
NC_000001.9:g.115049571A=	NCBI36
NG_007572.1:g.16468T= , LRG_92:g.16468T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2667T= MANE Select	ENSP00000358548.4:n.*2667T=
ENST00000369535.4:c.*2667T=	ENSP00000358548.4:n.*2667T=
NM_002524.4:c.*2667T=	NP_002515.1:n.*2667T=
NM_002524.5:c.*2667T= MANE Select	NP_002515.1:n.*2667T=