Canonical Allele Identifier: CA983635154
Gene: ZPBP2 HGNC NCBI

Linked Data

dbSNP Id: rs2063367175

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872051_39872053del , CM000679.2:g.39872051_39872053del GRCh38
NC_000017.10:g.38028304_38028306del , CM000679.1:g.38028304_38028306del GRCh37
NC_000017.9:g.35281830_35281832del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.407-219_407-217del MANE Select ENSP00000335384.5:n.407-219_407-217del
ENST00000348931.8:c.407-219_407-217del ENSP00000335384.5:n.407-219_407-217del
ENST00000377940.3:c.341-219_341-217del ENSP00000367174.3:n.341-219_341-217del
ENST00000583811.5:c.53-219_53-217del ENSP00000462463.1:n.53-219_53-217del
ENST00000584588.5:c.406+426_406+428del ENSP00000462067.1:n.406+426_406+428del
NM_198844.2:c.341-219_341-217del NP_942141.2:n.341-219_341-217del
NM_199321.2:c.407-219_407-217del NP_955353.1:n.407-219_407-217del
XM_011524298.1:c.407-219_407-217del XP_011522600.1:n.407-219_407-217del
XR_002957959.1:n.598-219_598-217del
NM_198844.3:c.341-219_341-217del NP_942141.2:n.341-219_341-217del
NM_199321.3:c.407-219_407-217del MANE Select NP_955353.1:n.407-219_407-217del