Canonical Allele Identifier: CA1190289649

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114710069T= , CM000663.2:g.114710069T=	GRCh38
NC_000001.10:g.115252690T= , CM000663.1:g.115252690T=	GRCh37
NC_000001.9:g.115054213T=	NCBI36
NG_007572.1:g.11826A= , LRG_92:g.11826A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.291-341A= MANE Select	ENSP00000358548.4:n.291-341A=
ENST00000369535.4:c.291-341A=	ENSP00000358548.4:n.291-341A=
NM_002524.4:c.291-341A=	NP_002515.1:n.291-341A=
NM_002524.5:c.291-341A= MANE Select	NP_002515.1:n.291-341A=