Canonical Allele Identifier: CA2745134562
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714018_114714019insGGGGCCAGGGTGGTAGGGAAG , CM000663.2:g.114714018_114714019insGGGGCCAGGGTGGTAGGGAAG GRCh38
NC_000001.10:g.115256639_115256640insGGGGCCAGGGTGGTAGGGAAG , CM000663.1:g.115256639_115256640insGGGGCCAGGGTGGTAGGGAAG GRCh37
NC_000001.9:g.115058162_115058163insGGGGCCAGGGTGGTAGGGAAG NCBI36
NG_007572.1:g.7883_7884insACCACCCTGGCCCCCTTCCCT , LRG_92:g.7883_7884insACCACCCTGGCCCCCTTCCCT

Transcript Alleles

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