Canonical Allele Identifier: CA2638881139

Gene: NOG

Linked Data

• gnomAD v4: 17-56595149-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595150_56595151del , CM000679.2:g.56595150_56595151del	GRCh38
NC_000017.10:g.54672511_54672512del , CM000679.1:g.54672511_54672512del	GRCh37
NC_000017.9:g.52027510_52027511del	NCBI36
NG_011958.1:g.6452_6453del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*228_*229del MANE Select	ENSP00000328181.4:n.*228_*229del
ENST00000332822.4:c.*228_*229del	ENSP00000328181.4:n.*228_*229del
NM_005450.4:c.*228_*229del	NP_005441.1:n.*228_*229del
NM_005450.6:c.*228_*229del MANE Select	NP_005441.1:n.*228_*229del