Canonical Allele Identifier: CA984892825

Gene: NOG

Linked Data

• gnomAD v3: 17-56595031-C-CCTTT
• gnomAD v4: 17-56595031-C-CCTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595031_56595032insCTTT , CM000679.2:g.56595031_56595032insCTTT	GRCh38
NC_000017.10:g.54672392_54672393insCTTT , CM000679.1:g.54672392_54672393insCTTT	GRCh37
NC_000017.9:g.52027391_52027392insCTTT	NCBI36
NG_011958.1:g.6333_6334insCTTT

Transcript Alleles

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