Canonical Allele Identifier: CA2647248601
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714011_114714012insT , CM000663.2:g.114714011_114714012insT GRCh38
NC_000001.10:g.115256632_115256633insT , CM000663.1:g.115256632_115256633insT GRCh37
NC_000001.9:g.115058155_115058156insT NCBI36
NG_007572.1:g.7883_7884insA , LRG_92:g.7883_7884insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-34_112-33insA MANE Select ENSP00000358548.4:n.112-34_112-33insA
ENST00000369535.4:c.112-34_112-33insA ENSP00000358548.4:n.112-34_112-33insA
NM_002524.4:c.112-34_112-33insA NP_002515.1:n.112-34_112-33insA
NM_002524.5:c.112-34_112-33insA MANE Select NP_002515.1:n.112-34_112-33insA