Canonical Allele Identifier: CA984892699

Gene: NOG

Linked Data

• dbSNP Id: rs2052473612
• gnomAD v3: 17-56594991-C-CAA
• gnomAD v4: 17-56594991-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56594992_56594993dup , CM000679.2:g.56594992_56594993dup	GRCh38
NC_000017.10:g.54672353_54672354dup , CM000679.1:g.54672353_54672354dup	GRCh37
NC_000017.9:g.52027352_52027353dup	NCBI36
NG_011958.1:g.6294_6295dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*70_*71dup MANE Select	ENSP00000328181.4:n.*70_*71dup
ENST00000332822.4:c.*70_*71dup	ENSP00000328181.4:n.*70_*71dup
NM_005450.4:c.*70_*71dup	NP_005441.1:n.*70_*71dup
NM_005450.6:c.*70_*71dup MANE Select	NP_005441.1:n.*70_*71dup