Canonical Allele Identifier: CA2259291000

Gene: ZPBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872658_39872662delinsCTAAT , CM000679.2:g.39872658_39872662delinsCTAAT	GRCh38
NC_000017.10:g.38028911_38028915delinsCTAAT , CM000679.1:g.38028911_38028915delinsCTAAT	GRCh37
NC_000017.9:g.35282437_35282441delinsCTAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.625+170_625+174delinsCTAAT MANE Select	ENSP00000335384.5:n.625+170_625+174delinsCTAAT
ENST00000348931.8:c.625+170_625+174delinsCTAAT	ENSP00000335384.5:n.625+170_625+174delinsCTAAT
ENST00000377940.3:c.559+170_559+174delinsCTAAT	ENSP00000367174.3:n.559+170_559+174delinsCTAAT
ENST00000583811.5:c.271+170_271+174delinsCTAAT	ENSP00000462463.1:n.271+170_271+174delinsCTAAT
ENST00000584588.5:c.407-386_407-382delinsCTAAT	ENSP00000462067.1:n.407-386_407-382delinsCTAAT
NM_198844.2:c.559+170_559+174delinsCTAAT	NP_942141.2:n.559+170_559+174delinsCTAAT
NM_199321.2:c.625+170_625+174delinsCTAAT	NP_955353.1:n.625+170_625+174delinsCTAAT
XM_011524298.1:c.625+170_625+174delinsCTAAT	XP_011522600.1:n.625+170_625+174delinsCTAAT
XR_002957959.1:n.816+170_816+174delinsCTAAT
NM_198844.3:c.559+170_559+174delinsCTAAT	NP_942141.2:n.559+170_559+174delinsCTAAT
NM_199321.3:c.625+170_625+174delinsCTAAT MANE Select	NP_955353.1:n.625+170_625+174delinsCTAAT