Canonical Allele Identifier: CA2647248519
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713997_114713998insCC , CM000663.2:g.114713997_114713998insCC GRCh38
NC_000001.10:g.115256618_115256619insCC , CM000663.1:g.115256618_115256619insCC GRCh37
NC_000001.9:g.115058141_115058142insCC NCBI36
NG_007572.1:g.7897_7898insGG , LRG_92:g.7897_7898insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-20_112-19insGG MANE Select ENSP00000358548.4:n.112-20_112-19insGG
ENST00000369535.4:c.112-20_112-19insGG ENSP00000358548.4:n.112-20_112-19insGG
NM_002524.4:c.112-20_112-19insGG NP_002515.1:n.112-20_112-19insGG
NM_002524.5:c.112-20_112-19insGG MANE Select NP_002515.1:n.112-20_112-19insGG