Canonical Allele Identifier: CA1190289414

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709442_114709443delinsAT , CM000663.2:g.114709442_114709443delinsAT	GRCh38
NC_000001.10:g.115252063_115252064delinsAT , CM000663.1:g.115252063_115252064delinsAT	GRCh37
NC_000001.9:g.115053586_115053587delinsAT	NCBI36
NG_007572.1:g.12452_12453delinsAT , LRG_92:g.12452_12453delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+126_450+127delinsAT MANE Select	ENSP00000358548.4:n.450+126_450+127delinsAT
ENST00000369535.4:c.450+126_450+127delinsAT	ENSP00000358548.4:n.450+126_450+127delinsAT
NM_002524.4:c.450+126_450+127delinsAT	NP_002515.1:n.450+126_450+127delinsAT
NM_002524.5:c.450+126_450+127delinsAT MANE Select	NP_002515.1:n.450+126_450+127delinsAT