Canonical Allele Identifier: CA2647248552
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114714002-G-GCC
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714003_114714004insCC , CM000663.2:g.114714003_114714004insCC GRCh38
NC_000001.10:g.115256624_115256625insCC , CM000663.1:g.115256624_115256625insCC GRCh37
NC_000001.9:g.115058147_115058148insCC NCBI36
NG_007572.1:g.7892_7893insGG , LRG_92:g.7892_7893insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-25_112-24insGG MANE Select ENSP00000358548.4:n.112-25_112-24insGG
ENST00000369535.4:c.112-25_112-24insGG ENSP00000358548.4:n.112-25_112-24insGG
NM_002524.4:c.112-25_112-24insGG NP_002515.1:n.112-25_112-24insGG
NM_002524.5:c.112-25_112-24insGG MANE Select NP_002515.1:n.112-25_112-24insGG
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