Canonical Allele Identifier: CA2647248629
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714015_114714016insC , CM000663.2:g.114714015_114714016insC GRCh38
NC_000001.10:g.115256636_115256637insC , CM000663.1:g.115256636_115256637insC GRCh37
NC_000001.9:g.115058159_115058160insC NCBI36
NG_007572.1:g.7879_7880insG , LRG_92:g.7879_7880insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-38_112-37insG MANE Select ENSP00000358548.4:n.112-38_112-37insG
ENST00000369535.4:c.112-38_112-37insG ENSP00000358548.4:n.112-38_112-37insG
NM_002524.4:c.112-38_112-37insG NP_002515.1:n.112-38_112-37insG
NM_002524.5:c.112-38_112-37insG MANE Select NP_002515.1:n.112-38_112-37insG