Canonical Allele Identifier: CA2638881160

Gene: NOG

Linked Data

• gnomAD v4: 17-56595179-C-CCT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595179_56595180insCT , CM000679.2:g.56595179_56595180insCT	GRCh38
NC_000017.10:g.54672540_54672541insCT , CM000679.1:g.54672540_54672541insCT	GRCh37
NC_000017.9:g.52027539_52027540insCT	NCBI36
NG_011958.1:g.6481_6482insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*257_*258insCT MANE Select	ENSP00000328181.4:n.*257_*258insCT
ENST00000332822.4:c.*257_*258insCT	ENSP00000328181.4:n.*257_*258insCT
NM_005450.4:c.*257_*258insCT	NP_005441.1:n.*257_*258insCT
NM_005450.6:c.*257_*258insCT MANE Select	NP_005441.1:n.*257_*258insCT