Canonical Allele Identifier: CA1190289412

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709441A= , CM000663.2:g.114709441A=	GRCh38
NC_000001.10:g.115252062A= , CM000663.1:g.115252062A=	GRCh37
NC_000001.9:g.115053585A=	NCBI36
NG_007572.1:g.12454T= , LRG_92:g.12454T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+128T= MANE Select	ENSP00000358548.4:n.450+128T=
ENST00000369535.4:c.450+128T=	ENSP00000358548.4:n.450+128T=
NM_002524.4:c.450+128T=	NP_002515.1:n.450+128T=
NM_002524.5:c.450+128T= MANE Select	NP_002515.1:n.450+128T=