Canonical Allele Identifier: CA1190289646

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114710060A= , CM000663.2:g.114710060A=	GRCh38
NC_000001.10:g.115252681A= , CM000663.1:g.115252681A=	GRCh37
NC_000001.9:g.115054204A=	NCBI36
NG_007572.1:g.11835T= , LRG_92:g.11835T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.291-332T= MANE Select	ENSP00000358548.4:n.291-332T=
ENST00000369535.4:c.291-332T=	ENSP00000358548.4:n.291-332T=
NM_002524.4:c.291-332T=	NP_002515.1:n.291-332T=
NM_002524.5:c.291-332T= MANE Select	NP_002515.1:n.291-332T=