Canonical Allele Identifier: CA2809927362
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595056_56595057insAT , CM000679.2:g.56595056_56595057insAT GRCh38
NC_000017.10:g.54672417_54672418insAT , CM000679.1:g.54672417_54672418insAT GRCh37
NC_000017.9:g.52027416_52027417insAT NCBI36
NG_011958.1:g.6358_6359insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*134_*135insAT MANE Select ENSP00000328181.4:n.*134_*135insAT
ENST00000332822.4:c.*134_*135insAT ENSP00000328181.4:n.*134_*135insAT
NM_005450.4:c.*134_*135insAT NP_005441.1:n.*134_*135insAT
NM_005450.6:c.*134_*135insAT MANE Select NP_005441.1:n.*134_*135insAT