Canonical Allele Identifier: CA1190289650

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114710074C= , CM000663.2:g.114710074C=	GRCh38
NC_000001.10:g.115252695C= , CM000663.1:g.115252695C=	GRCh37
NC_000001.9:g.115054218C=	NCBI36
NG_007572.1:g.11821G= , LRG_92:g.11821G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.291-346G= MANE Select	ENSP00000358548.4:n.291-346G=
ENST00000369535.4:c.291-346G=	ENSP00000358548.4:n.291-346G=
NM_002524.4:c.291-346G=	NP_002515.1:n.291-346G=
NM_002524.5:c.291-346G= MANE Select	NP_002515.1:n.291-346G=