Canonical Allele Identifier: CA2637649535

Gene: ZPBP2

Linked Data

• gnomAD v4: 17-39872255-C-CTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872261_39872265dup , CM000679.2:g.39872261_39872265dup	GRCh38
NC_000017.10:g.38028514_38028518dup , CM000679.1:g.38028514_38028518dup	GRCh37
NC_000017.9:g.35282040_35282044dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.407-9_407-5dup MANE Select	ENSP00000335384.5:n.407-9_407-5dup
ENST00000348931.8:c.407-9_407-5dup	ENSP00000335384.5:n.407-9_407-5dup
ENST00000377940.3:c.341-9_341-5dup	ENSP00000367174.3:n.341-9_341-5dup
ENST00000583811.5:c.53-9_53-5dup	ENSP00000462463.1:n.53-9_53-5dup
ENST00000584588.5:c.406+636_406+640dup	ENSP00000462067.1:n.406+636_406+640dup
NM_198844.2:c.341-9_341-5dup	NP_942141.2:n.341-9_341-5dup
NM_199321.2:c.407-9_407-5dup	NP_955353.1:n.407-9_407-5dup
XM_011524298.1:c.407-9_407-5dup	XP_011522600.1:n.407-9_407-5dup
XR_002957959.1:n.598-9_598-5dup
NM_198844.3:c.341-9_341-5dup	NP_942141.2:n.341-9_341-5dup
NM_199321.3:c.407-9_407-5dup MANE Select	NP_955353.1:n.407-9_407-5dup