Canonical Allele Identifier: CA2266876419
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594956_56594957delinsTG , CM000679.2:g.56594956_56594957delinsTG GRCh38
NC_000017.10:g.54672317_54672318delinsTG , CM000679.1:g.54672317_54672318delinsTG GRCh37
NC_000017.9:g.52027316_52027317delinsTG NCBI36
NG_011958.1:g.6258_6259delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*34_*35delinsTG MANE Select ENSP00000328181.4:n.*34_*35delinsTG
ENST00000332822.4:c.*34_*35delinsTG ENSP00000328181.4:n.*34_*35delinsTG
NM_005450.4:c.*34_*35delinsTG NP_005441.1:n.*34_*35delinsTG
NM_005450.6:c.*34_*35delinsTG MANE Select NP_005441.1:n.*34_*35delinsTG