Canonical Allele Identifier: CA2638881045

Gene: NOG

Linked Data

• gnomAD v4: 17-56595031-C-CCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595031_56595032insCTT , CM000679.2:g.56595031_56595032insCTT	GRCh38
NC_000017.10:g.54672392_54672393insCTT , CM000679.1:g.54672392_54672393insCTT	GRCh37
NC_000017.9:g.52027391_52027392insCTT	NCBI36
NG_011958.1:g.6333_6334insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*109_*110insCTT MANE Select	ENSP00000328181.4:n.*109_*110insCTT
ENST00000332822.4:c.*109_*110insCTT	ENSP00000328181.4:n.*109_*110insCTT
NM_005450.4:c.*109_*110insCTT	NP_005441.1:n.*109_*110insCTT
NM_005450.6:c.*109_*110insCTT MANE Select	NP_005441.1:n.*109_*110insCTT