Canonical Allele Identifier: CA2637649450

Gene: ZPBP2

Linked Data

• gnomAD v4: 17-39872225-C-CTAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872228_39872231dup , CM000679.2:g.39872228_39872231dup	GRCh38
NC_000017.10:g.38028481_38028484dup , CM000679.1:g.38028481_38028484dup	GRCh37
NC_000017.9:g.35282007_35282010dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000348931.9:c.407-42_407-39dup MANE Select	ENSP00000335384.5:n.407-42_407-39dup
ENST00000348931.8:c.407-42_407-39dup	ENSP00000335384.5:n.407-42_407-39dup
ENST00000377940.3:c.341-42_341-39dup	ENSP00000367174.3:n.341-42_341-39dup
ENST00000583811.5:c.53-42_53-39dup	ENSP00000462463.1:n.53-42_53-39dup
ENST00000584588.5:c.406+603_406+606dup	ENSP00000462067.1:n.406+603_406+606dup
NM_198844.2:c.341-42_341-39dup	NP_942141.2:n.341-42_341-39dup
NM_199321.2:c.407-42_407-39dup	NP_955353.1:n.407-42_407-39dup
XM_011524298.1:c.407-42_407-39dup	XP_011522600.1:n.407-42_407-39dup
XR_002957959.1:n.598-42_598-39dup
NM_198844.3:c.341-42_341-39dup	NP_942141.2:n.341-42_341-39dup
NM_199321.3:c.407-42_407-39dup MANE Select	NP_955353.1:n.407-42_407-39dup