Canonical Allele Identifier: CA2696725952

Gene: NRAS

Linked Data

• dbSNP Id: rs2101741444

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713424_114713425insC , CM000663.2:g.114713424_114713425insC	GRCh38
NC_000001.10:g.115256045_115256046insC , CM000663.1:g.115256045_115256046insC	GRCh37
NC_000001.9:g.115057568_115057569insC	NCBI36
NG_007572.1:g.8470_8471insG , LRG_92:g.8470_8471insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+375_290+376insG MANE Select	ENSP00000358548.4:n.290+375_290+376insG
ENST00000369535.4:c.290+375_290+376insG	ENSP00000358548.4:n.290+375_290+376insG
NM_002524.4:c.290+375_290+376insG	NP_002515.1:n.290+375_290+376insG
NM_002524.5:c.290+375_290+376insG MANE Select	NP_002515.1:n.290+375_290+376insG