Canonical Allele Identifier: CA1190291360

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114714059G= , CM000663.2:g.114714059G=	GRCh38
NC_000001.10:g.115256680G= , CM000663.1:g.115256680G=	GRCh37
NC_000001.9:g.115058203G=	NCBI36
NG_007572.1:g.7836C= , LRG_92:g.7836C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-81C= MANE Select	ENSP00000358548.4:n.112-81C=
ENST00000369535.4:c.112-81C=	ENSP00000358548.4:n.112-81C=
NM_002524.4:c.112-81C=	NP_002515.1:n.112-81C=
NM_002524.5:c.112-81C= MANE Select	NP_002515.1:n.112-81C=