Canonical Allele Identifier: CA2638881040
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595030_56595031insATT , CM000679.2:g.56595030_56595031insATT GRCh38
NC_000017.10:g.54672391_54672392insATT , CM000679.1:g.54672391_54672392insATT GRCh37
NC_000017.9:g.52027390_52027391insATT NCBI36
NG_011958.1:g.6332_6333insATT

Transcript Alleles

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