Canonical Allele Identifier: CA1190284330

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705307G= , CM000663.2:g.114705307G=	GRCh38
NC_000001.10:g.115247928G= , CM000663.1:g.115247928G=	GRCh37
NC_000001.9:g.115049451G=	NCBI36
NG_007572.1:g.16588C= , LRG_92:g.16588C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2787C= MANE Select	ENSP00000358548.4:n.*2787C=
ENST00000369535.4:c.*2787C=	ENSP00000358548.4:n.*2787C=
NM_002524.4:c.*2787C=	NP_002515.1:n.*2787C=
NM_002524.5:c.*2787C= MANE Select	NP_002515.1:n.*2787C=