Canonical Allele Identifier: CA1190291181

Gene: NRAS

Linked Data

• dbSNP Id: rs1659087557

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713487dup , CM000663.2:g.114713487dup	GRCh38
NC_000001.10:g.115256108dup , CM000663.1:g.115256108dup	GRCh37
NC_000001.9:g.115057631dup	NCBI36
NG_007572.1:g.8410dup , LRG_92:g.8410dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+315dup MANE Select	ENSP00000358548.4:n.290+315dup
ENST00000369535.4:c.290+315dup	ENSP00000358548.4:n.290+315dup
NM_002524.4:c.290+315dup	NP_002515.1:n.290+315dup
NM_002524.5:c.290+315dup MANE Select	NP_002515.1:n.290+315dup