Canonical Allele Identifier: CA1190291227

Gene: NRAS

Linked Data

• dbSNP Id: rs1659090288

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713653_114713654insCTAGATTCTAGATTCTAG , CM000663.2:g.114713653_114713654insCTAGATTCTAGATTCTAG	GRCh38
NC_000001.10:g.115256274_115256275insCTAGATTCTAGATTCTAG , CM000663.1:g.115256274_115256275insCTAGATTCTAGATTCTAG	GRCh37
NC_000001.9:g.115057797_115057798insCTAGATTCTAGATTCTAG	NCBI36
NG_007572.1:g.8241_8242insCTAGAATCTAGAATCTAG , LRG_92:g.8241_8242insCTAGAATCTAGAATCTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+146_290+147insCTAGAATCTAGAATCTAG MANE Select	ENSP00000358548.4:n.290+146_290+147insCTAGAATCTAGAATCTAG
ENST00000369535.4:c.290+146_290+147insCTAGAATCTAGAATCTAG	ENSP00000358548.4:n.290+146_290+147insCTAGAATCTAGAATCTAG
NM_002524.4:c.290+146_290+147insCTAGAATCTAGAATCTAG	NP_002515.1:n.290+146_290+147insCTAGAATCTAGAATCTAG
NM_002524.5:c.290+146_290+147insCTAGAATCTAGAATCTAG MANE Select	NP_002515.1:n.290+146_290+147insCTAGAATCTAGAATCTAG