Canonical Allele Identifier: CA1190285524

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114706898G= , CM000663.2:g.114706898G=	GRCh38
NC_000001.10:g.115249519G= , CM000663.1:g.115249519G=	GRCh37
NC_000001.9:g.115051042G=	NCBI36
NG_007572.1:g.14997C= , LRG_92:g.14997C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*1196C= MANE Select	ENSP00000358548.4:n.*1196C=
ENST00000369535.4:c.*1196C=	ENSP00000358548.4:n.*1196C=
NM_002524.4:c.*1196C=	NP_002515.1:n.*1196C=
NM_002524.5:c.*1196C= MANE Select	NP_002515.1:n.*1196C=