Canonical Allele Identifier: CA1190289379

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709377G= , CM000663.2:g.114709377G=	GRCh38
NC_000001.10:g.115251998G= , CM000663.1:g.115251998G=	GRCh37
NC_000001.9:g.115053521G=	NCBI36
NG_007572.1:g.12518C= , LRG_92:g.12518C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+192C= MANE Select	ENSP00000358548.4:n.450+192C=
ENST00000369535.4:c.450+192C=	ENSP00000358548.4:n.450+192C=
NM_002524.4:c.450+192C=	NP_002515.1:n.450+192C=
NM_002524.5:c.450+192C= MANE Select	NP_002515.1:n.450+192C=