Canonical Allele Identifier: CA1190289001

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114708103C= , CM000663.2:g.114708103C=	GRCh38
NC_000001.10:g.115250724C= , CM000663.1:g.115250724C=	GRCh37
NC_000001.9:g.115052247C=	NCBI36
NG_007572.1:g.13792G= , LRG_92:g.13792G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*43+51G= MANE Select	ENSP00000358548.4:n.*43+51G=
ENST00000369535.4:c.*43+51G=	ENSP00000358548.4:n.*43+51G=
NM_002524.4:c.*43+51G=	NP_002515.1:n.*43+51G=
NM_002524.5:c.*43+51G= MANE Select	NP_002515.1:n.*43+51G=