Canonical Allele Identifier: CA1190291155

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713419C= , CM000663.2:g.114713419C=	GRCh38
NC_000001.10:g.115256040C= , CM000663.1:g.115256040C=	GRCh37
NC_000001.9:g.115057563C=	NCBI36
NG_007572.1:g.8476G= , LRG_92:g.8476G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+381G= MANE Select	ENSP00000358548.4:n.290+381G=
ENST00000369535.4:c.290+381G=	ENSP00000358548.4:n.290+381G=
NM_002524.4:c.290+381G=	NP_002515.1:n.290+381G=
NM_002524.5:c.290+381G= MANE Select	NP_002515.1:n.290+381G=