Canonical Allele Identifier: CA1190291165

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713454G= , CM000663.2:g.114713454G=	GRCh38
NC_000001.10:g.115256075G= , CM000663.1:g.115256075G=	GRCh37
NC_000001.9:g.115057598G=	NCBI36
NG_007572.1:g.8441C= , LRG_92:g.8441C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+346C= MANE Select	ENSP00000358548.4:n.290+346C=
ENST00000369535.4:c.290+346C=	ENSP00000358548.4:n.290+346C=
NM_002524.4:c.290+346C=	NP_002515.1:n.290+346C=
NM_002524.5:c.290+346C= MANE Select	NP_002515.1:n.290+346C=