Canonical Allele Identifier: CA2647253727
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709731_114709732insCTGACTG , CM000663.2:g.114709731_114709732insCTGACTG GRCh38
NC_000001.10:g.115252352_115252353insCTGACTG , CM000663.1:g.115252352_115252353insCTGACTG GRCh37
NC_000001.9:g.115053875_115053876insCTGACTG NCBI36
NG_007572.1:g.12163_12164insCAGTCAG , LRG_92:g.12163_12164insCAGTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-4_291-3insCAGTCAG MANE Select ENSP00000358548.4:n.291-4_291-3insCAGTCAG
ENST00000369535.4:c.291-4_291-3insCAGTCAG ENSP00000358548.4:n.291-4_291-3insCAGTCAG
NM_002524.4:c.291-4_291-3insCAGTCAG NP_002515.1:n.291-4_291-3insCAGTCAG
NM_002524.5:c.291-4_291-3insCAGTCAG MANE Select NP_002515.1:n.291-4_291-3insCAGTCAG