Canonical Allele Identifier: CA2647248393
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713984_114713985del , CM000663.2:g.114713984_114713985del GRCh38
NC_000001.10:g.115256605_115256606del , CM000663.1:g.115256605_115256606del GRCh37
NC_000001.9:g.115058128_115058129del NCBI36
NG_007572.1:g.7913_7914del , LRG_92:g.7913_7914del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-4_112-3del MANE Select ENSP00000358548.4:n.112-4_112-3del
ENST00000369535.4:c.112-4_112-3del ENSP00000358548.4:n.112-4_112-3del
NM_002524.4:c.112-4_112-3del NP_002515.1:n.112-4_112-3del
NM_002524.5:c.112-4_112-3del MANE Select NP_002515.1:n.112-4_112-3del