Canonical Allele Identifier: CA2259290904

Gene: ZPBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872431_39872442delinsCATTCTGTTGAA , CM000679.2:g.39872431_39872442delinsCATTCTGTTGAA	GRCh38
NC_000017.10:g.38028684_38028695delinsCATTCTGTTGAA , CM000679.1:g.38028684_38028695delinsCATTCTGTTGAA	GRCh37
NC_000017.9:g.35282210_35282221delinsCATTCTGTTGAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.568_579delinsCATTCTGTTGAA MANE Select	ENSP00000335384.5:p.His190=
ENST00000348931.8:c.568_579delinsCATTCTGTTGAA	ENSP00000335384.5:p.His190=
ENST00000377940.3:c.502_513delinsCATTCTGTTGAA	ENSP00000367174.3:p.His168=
ENST00000583811.5:c.214_225delinsCATTCTGTTGAA	ENSP00000462463.1:p.His72=
ENST00000584588.5:c.407-613_407-602delinsCATTCTGTTGAA	ENSP00000462067.1:n.407-613_407-602delinsCATTCTGTTGAA
NM_198844.2:c.502_513delinsCATTCTGTTGAA	NP_942141.2:p.His168=
NM_199321.2:c.568_579delinsCATTCTGTTGAA	NP_955353.1:p.His190=
XM_011524298.1:c.568_579delinsCATTCTGTTGAA	XP_011522600.1:p.His190=
XR_002957959.1:n.759_770delinsCATTCTGTTGAA
NM_198844.3:c.502_513delinsCATTCTGTTGAA	NP_942141.2:p.His168=
NM_199321.3:c.568_579delinsCATTCTGTTGAA MANE Select	NP_955353.1:p.His190=