Canonical Allele Identifier: CA2638881108

Gene: NOG

Linked Data

• gnomAD v4: 17-56595116-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595116_56595117insC , CM000679.2:g.56595116_56595117insC	GRCh38
NC_000017.10:g.54672477_54672478insC , CM000679.1:g.54672477_54672478insC	GRCh37
NC_000017.9:g.52027476_52027477insC	NCBI36
NG_011958.1:g.6418_6419insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*194_*195insC MANE Select	ENSP00000328181.4:n.*194_*195insC
ENST00000332822.4:c.*194_*195insC	ENSP00000328181.4:n.*194_*195insC
NM_005450.4:c.*194_*195insC	NP_005441.1:n.*194_*195insC
NM_005450.6:c.*194_*195insC MANE Select	NP_005441.1:n.*194_*195insC