Canonical Allele Identifier: CA1190285681

Gene: NRAS

Linked Data

• dbSNP Id: rs1658935312

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114707089del , CM000663.2:g.114707089del	GRCh38
NC_000001.10:g.115249710del , CM000663.1:g.115249710del	GRCh37
NC_000001.9:g.115051233del	NCBI36
NG_007572.1:g.14808del , LRG_92:g.14808del

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.*1007del MANE Select	ENSP00000358548.4:n.*1007del
ENST00000369535.4:c.*1007del	ENSP00000358548.4:n.*1007del
NM_002524.4:c.*1007del	NP_002515.1:n.*1007del
NM_002524.5:c.*1007del MANE Select	NP_002515.1:n.*1007del