Canonical Allele Identifier: CA2809927355
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595030_56595031insATTTTT , CM000679.2:g.56595030_56595031insATTTTT GRCh38
NC_000017.10:g.54672391_54672392insATTTTT , CM000679.1:g.54672391_54672392insATTTTT GRCh37
NC_000017.9:g.52027390_52027391insATTTTT NCBI36
NG_011958.1:g.6332_6333insATTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*108_*109insATTTTT MANE Select ENSP00000328181.4:n.*108_*109insATTTTT
ENST00000332822.4:c.*108_*109insATTTTT ENSP00000328181.4:n.*108_*109insATTTTT
NM_005450.4:c.*108_*109insATTTTT NP_005441.1:n.*108_*109insATTTTT
NM_005450.6:c.*108_*109insATTTTT MANE Select NP_005441.1:n.*108_*109insATTTTT