Canonical Allele Identifier: CA1190291174

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713475_114713479delinsTTACA , CM000663.2:g.114713475_114713479delinsTTACA	GRCh38
NC_000001.10:g.115256096_115256100delinsTTACA , CM000663.1:g.115256096_115256100delinsTTACA	GRCh37
NC_000001.9:g.115057619_115057623delinsTTACA	NCBI36
NG_007572.1:g.8416_8420delinsTGTAA , LRG_92:g.8416_8420delinsTGTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+321_290+325delinsTGTAA MANE Select	ENSP00000358548.4:n.290+321_290+325delinsTGTAA
ENST00000369535.4:c.290+321_290+325delinsTGTAA	ENSP00000358548.4:n.290+321_290+325delinsTGTAA
NM_002524.4:c.290+321_290+325delinsTGTAA	NP_002515.1:n.290+321_290+325delinsTGTAA
NM_002524.5:c.290+321_290+325delinsTGTAA MANE Select	NP_002515.1:n.290+321_290+325delinsTGTAA