Canonical Allele Identifier: CA2259290776

Gene: ZPBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872141_39872144delinsCGTT , CM000679.2:g.39872141_39872144delinsCGTT	GRCh38
NC_000017.10:g.38028394_38028397delinsCGTT , CM000679.1:g.38028394_38028397delinsCGTT	GRCh37
NC_000017.9:g.35281920_35281923delinsCGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.407-129_407-126delinsCGTT MANE Select	ENSP00000335384.5:n.407-129_407-126delinsCGTT
ENST00000348931.8:c.407-129_407-126delinsCGTT	ENSP00000335384.5:n.407-129_407-126delinsCGTT
ENST00000377940.3:c.341-129_341-126delinsCGTT	ENSP00000367174.3:n.341-129_341-126delinsCGTT
ENST00000583811.5:c.53-129_53-126delinsCGTT	ENSP00000462463.1:n.53-129_53-126delinsCGTT
ENST00000584588.5:c.406+516_406+519delinsCGTT	ENSP00000462067.1:n.406+516_406+519delinsCGTT
NM_198844.2:c.341-129_341-126delinsCGTT	NP_942141.2:n.341-129_341-126delinsCGTT
NM_199321.2:c.407-129_407-126delinsCGTT	NP_955353.1:n.407-129_407-126delinsCGTT
XM_011524298.1:c.407-129_407-126delinsCGTT	XP_011522600.1:n.407-129_407-126delinsCGTT
XR_002957959.1:n.598-129_598-126delinsCGTT
NM_198844.3:c.341-129_341-126delinsCGTT	NP_942141.2:n.341-129_341-126delinsCGTT
NM_199321.3:c.407-129_407-126delinsCGTT MANE Select	NP_955353.1:n.407-129_407-126delinsCGTT