Canonical Allele Identifier: CA1190284854

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705943A= , CM000663.2:g.114705943A=	GRCh38
NC_000001.10:g.115248564A= , CM000663.1:g.115248564A=	GRCh37
NC_000001.9:g.115050087A=	NCBI36
NG_007572.1:g.15952T= , LRG_92:g.15952T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2151T= MANE Select	ENSP00000358548.4:n.*2151T=
ENST00000369535.4:c.*2151T=	ENSP00000358548.4:n.*2151T=
NM_002524.4:c.*2151T=	NP_002515.1:n.*2151T=
NM_002524.5:c.*2151T= MANE Select	NP_002515.1:n.*2151T=