Canonical Allele Identifier: CA1190289418

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709443_114709447delinsTAAAA , CM000663.2:g.114709443_114709447delinsTAAAA	GRCh38
NC_000001.10:g.115252064_115252068delinsTAAAA , CM000663.1:g.115252064_115252068delinsTAAAA	GRCh37
NC_000001.9:g.115053587_115053591delinsTAAAA	NCBI36
NG_007572.1:g.12448_12452delinsTTTTA , LRG_92:g.12448_12452delinsTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+122_450+126delinsTTTTA MANE Select	ENSP00000358548.4:n.450+122_450+126delinsTTTTA
ENST00000369535.4:c.450+122_450+126delinsTTTTA	ENSP00000358548.4:n.450+122_450+126delinsTTTTA
NM_002524.4:c.450+122_450+126delinsTTTTA	NP_002515.1:n.450+122_450+126delinsTTTTA
NM_002524.5:c.450+122_450+126delinsTTTTA MANE Select	NP_002515.1:n.450+122_450+126delinsTTTTA