Canonical Allele Identifier: CA2696725953

Gene: NRAS

Linked Data

• dbSNP Id: rs2101741456

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713470_114713471del , CM000663.2:g.114713470_114713471del	GRCh38
NC_000001.10:g.115256091_115256092del , CM000663.1:g.115256091_115256092del	GRCh37
NC_000001.9:g.115057614_115057615del	NCBI36
NG_007572.1:g.8426_8427del , LRG_92:g.8426_8427del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+331_290+332del MANE Select	ENSP00000358548.4:n.290+331_290+332del
ENST00000369535.4:c.290+331_290+332del	ENSP00000358548.4:n.290+331_290+332del
NM_002524.4:c.290+331_290+332del	NP_002515.1:n.290+331_290+332del
NM_002524.5:c.290+331_290+332del MANE Select	NP_002515.1:n.290+331_290+332del