Canonical Allele Identifier: CA1190284668

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705692T= , CM000663.2:g.114705692T=	GRCh38
NC_000001.10:g.115248313T= , CM000663.1:g.115248313T=	GRCh37
NC_000001.9:g.115049836T=	NCBI36
NG_007572.1:g.16203A= , LRG_92:g.16203A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2402A= MANE Select	ENSP00000358548.4:n.*2402A=
ENST00000369535.4:c.*2402A=	ENSP00000358548.4:n.*2402A=
NM_002524.4:c.*2402A=	NP_002515.1:n.*2402A=
NM_002524.5:c.*2402A= MANE Select	NP_002515.1:n.*2402A=