Canonical Allele Identifier: CA2647248616
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714018_114714019insGGGGCCTGGGTGGGTGGGAAG , CM000663.2:g.114714018_114714019insGGGGCCTGGGTGGGTGGGAAG GRCh38
NC_000001.10:g.115256639_115256640insGGGGCCTGGGTGGGTGGGAAG , CM000663.1:g.115256639_115256640insGGGGCCTGGGTGGGTGGGAAG GRCh37
NC_000001.9:g.115058162_115058163insGGGGCCTGGGTGGGTGGGAAG NCBI36
NG_007572.1:g.7882_7883insACCCACCCAGGCCCCCTTCCC , LRG_92:g.7882_7883insACCCACCCAGGCCCCCTTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC MANE Select ENSP00000358548.4:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC
ENST00000369535.4:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC ENSP00000358548.4:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC
NM_002524.4:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC NP_002515.1:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC
NM_002524.5:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC MANE Select NP_002515.1:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC