Canonical Allele Identifier: CA1190291214

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713582_114713583delinsCT , CM000663.2:g.114713582_114713583delinsCT	GRCh38
NC_000001.10:g.115256203_115256204delinsCT , CM000663.1:g.115256203_115256204delinsCT	GRCh37
NC_000001.9:g.115057726_115057727delinsCT	NCBI36
NG_007572.1:g.8312_8313delinsAG , LRG_92:g.8312_8313delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+217_290+218delinsAG MANE Select	ENSP00000358548.4:n.290+217_290+218delinsAG
ENST00000369535.4:c.290+217_290+218delinsAG	ENSP00000358548.4:n.290+217_290+218delinsAG
NM_002524.4:c.290+217_290+218delinsAG	NP_002515.1:n.290+217_290+218delinsAG
NM_002524.5:c.290+217_290+218delinsAG MANE Select	NP_002515.1:n.290+217_290+218delinsAG