Canonical Allele Identifier: CA2259290715
Gene: ZPBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39871992_39871993delinsCT , CM000679.2:g.39871992_39871993delinsCT GRCh38
NC_000017.10:g.38028245_38028246delinsCT , CM000679.1:g.38028245_38028246delinsCT GRCh37
NC_000017.9:g.35281771_35281772delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.407-278_407-277delinsCT MANE Select ENSP00000335384.5:n.407-278_407-277delinsCT
ENST00000348931.8:c.407-278_407-277delinsCT ENSP00000335384.5:n.407-278_407-277delinsCT
ENST00000377940.3:c.341-278_341-277delinsCT ENSP00000367174.3:n.341-278_341-277delinsCT
ENST00000583811.5:c.53-278_53-277delinsCT ENSP00000462463.1:n.53-278_53-277delinsCT
ENST00000584588.5:c.406+367_406+368delinsCT ENSP00000462067.1:n.406+367_406+368delinsCT
NM_198844.2:c.341-278_341-277delinsCT NP_942141.2:n.341-278_341-277delinsCT
NM_199321.2:c.407-278_407-277delinsCT NP_955353.1:n.407-278_407-277delinsCT
XM_011524298.1:c.407-278_407-277delinsCT XP_011522600.1:n.407-278_407-277delinsCT
XR_002957959.1:n.598-278_598-277delinsCT
NM_198844.3:c.341-278_341-277delinsCT NP_942141.2:n.341-278_341-277delinsCT
NM_199321.3:c.407-278_407-277delinsCT MANE Select NP_955353.1:n.407-278_407-277delinsCT