Canonical Allele Identifier: CA2259290741
Gene: ZPBP2 HGNC NCBI

Linked Data

dbSNP Id: rs2063367138

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872042_39872043del , CM000679.2:g.39872042_39872043del GRCh38
NC_000017.10:g.38028295_38028296del , CM000679.1:g.38028295_38028296del GRCh37
NC_000017.9:g.35281821_35281822del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.407-228_407-227del MANE Select ENSP00000335384.5:n.407-228_407-227del
ENST00000348931.8:c.407-228_407-227del ENSP00000335384.5:n.407-228_407-227del
ENST00000377940.3:c.341-228_341-227del ENSP00000367174.3:n.341-228_341-227del
ENST00000583811.5:c.53-228_53-227del ENSP00000462463.1:n.53-228_53-227del
ENST00000584588.5:c.406+417_406+418del ENSP00000462067.1:n.406+417_406+418del
NM_198844.2:c.341-228_341-227del NP_942141.2:n.341-228_341-227del
NM_199321.2:c.407-228_407-227del NP_955353.1:n.407-228_407-227del
XM_011524298.1:c.407-228_407-227del XP_011522600.1:n.407-228_407-227del
XR_002957959.1:n.598-228_598-227del
NM_198844.3:c.341-228_341-227del NP_942141.2:n.341-228_341-227del
NM_199321.3:c.407-228_407-227del MANE Select NP_955353.1:n.407-228_407-227del