Canonical Allele Identifier: CA2266876483
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595030_56595034delinsACTTT , CM000679.2:g.56595030_56595034delinsACTTT GRCh38
NC_000017.10:g.54672391_54672395delinsACTTT , CM000679.1:g.54672391_54672395delinsACTTT GRCh37
NC_000017.9:g.52027390_52027394delinsACTTT NCBI36
NG_011958.1:g.6332_6336delinsACTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*108_*112delinsACTTT MANE Select ENSP00000328181.4:n.*108_*112delinsACTTT
ENST00000332822.4:c.*108_*112delinsACTTT ENSP00000328181.4:n.*108_*112delinsACTTT
NM_005450.4:c.*108_*112delinsACTTT NP_005441.1:n.*108_*112delinsACTTT
NM_005450.6:c.*108_*112delinsACTTT MANE Select NP_005441.1:n.*108_*112delinsACTTT