Canonical Allele Identifier: CA983635201

Gene: ZPBP2

Linked Data

• gnomAD v3: 17-39872080-A-AC
• gnomAD v4: 17-39872080-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872080_39872081insC , CM000679.2:g.39872080_39872081insC	GRCh38
NC_000017.10:g.38028333_38028334insC , CM000679.1:g.38028333_38028334insC	GRCh37
NC_000017.9:g.35281859_35281860insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.407-190_407-189insC MANE Select	ENSP00000335384.5:n.407-190_407-189insC
ENST00000348931.8:c.407-190_407-189insC	ENSP00000335384.5:n.407-190_407-189insC
ENST00000377940.3:c.341-190_341-189insC	ENSP00000367174.3:n.341-190_341-189insC
ENST00000583811.5:c.53-190_53-189insC	ENSP00000462463.1:n.53-190_53-189insC
ENST00000584588.5:c.406+455_406+456insC	ENSP00000462067.1:n.406+455_406+456insC
NM_198844.2:c.341-190_341-189insC	NP_942141.2:n.341-190_341-189insC
NM_199321.2:c.407-190_407-189insC	NP_955353.1:n.407-190_407-189insC
XM_011524298.1:c.407-190_407-189insC	XP_011522600.1:n.407-190_407-189insC
XR_002957959.1:n.598-190_598-189insC
NM_198844.3:c.341-190_341-189insC	NP_942141.2:n.341-190_341-189insC
NM_199321.3:c.407-190_407-189insC MANE Select	NP_955353.1:n.407-190_407-189insC