Canonical Allele Identifier: CA1190291215
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1659089441

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713584del , CM000663.2:g.114713584del GRCh38
NC_000001.10:g.115256205del , CM000663.1:g.115256205del GRCh37
NC_000001.9:g.115057728del NCBI36
NG_007572.1:g.8312del , LRG_92:g.8312del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+217del MANE Select ENSP00000358548.4:n.290+217del
ENST00000369535.4:c.290+217del ENSP00000358548.4:n.290+217del
NM_002524.4:c.290+217del NP_002515.1:n.290+217del
NM_002524.5:c.290+217del MANE Select NP_002515.1:n.290+217del