Canonical Allele Identifier: CA2647248543
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714003_114714009del , CM000663.2:g.114714003_114714009del GRCh38
NC_000001.10:g.115256624_115256630del , CM000663.1:g.115256624_115256630del GRCh37
NC_000001.9:g.115058147_115058153del NCBI36
NG_007572.1:g.7887_7893del , LRG_92:g.7887_7893del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-30_112-24del MANE Select ENSP00000358548.4:n.112-30_112-24del
ENST00000369535.4:c.112-30_112-24del ENSP00000358548.4:n.112-30_112-24del
NM_002524.4:c.112-30_112-24del NP_002515.1:n.112-30_112-24del
NM_002524.5:c.112-30_112-24del MANE Select NP_002515.1:n.112-30_112-24del