Canonical Allele Identifier: CA1147248010

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713537_114713540delinsATTA , CM000663.2:g.114713537_114713540delinsATTA	GRCh38
NC_000001.10:g.115256158_115256161delinsATTA , CM000663.1:g.115256158_115256161delinsATTA	GRCh37
NC_000001.9:g.115057681_115057684delinsATTA	NCBI36
NG_007572.1:g.8355_8358delinsTAAT , LRG_92:g.8355_8358delinsTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+260_290+263delinsTAAT MANE Select	ENSP00000358548.4:n.290+260_290+263delinsTAAT
ENST00000369535.4:c.290+260_290+263delinsTAAT	ENSP00000358548.4:n.290+260_290+263delinsTAAT
NM_002524.4:c.290+260_290+263delinsTAAT	NP_002515.1:n.290+260_290+263delinsTAAT
NM_002524.5:c.290+260_290+263delinsTAAT MANE Select	NP_002515.1:n.290+260_290+263delinsTAAT