Canonical Allele Identifier: CA2549602009

Gene: ZPBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872618_39872619del , CM000679.2:g.39872618_39872619del	GRCh38
NC_000017.10:g.38028871_38028872del , CM000679.1:g.38028871_38028872del	GRCh37
NC_000017.9:g.35282397_35282398del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.625+130_625+131del MANE Select	ENSP00000335384.5:n.625+130_625+131del
ENST00000348931.8:c.625+130_625+131del	ENSP00000335384.5:n.625+130_625+131del
ENST00000377940.3:c.559+130_559+131del	ENSP00000367174.3:n.559+130_559+131del
ENST00000583811.5:c.271+130_271+131del	ENSP00000462463.1:n.271+130_271+131del
ENST00000584588.5:c.407-426_407-425del	ENSP00000462067.1:n.407-426_407-425del
NM_198844.2:c.559+130_559+131del	NP_942141.2:n.559+130_559+131del
NM_199321.2:c.625+130_625+131del	NP_955353.1:n.625+130_625+131del
XM_011524298.1:c.625+130_625+131del	XP_011522600.1:n.625+130_625+131del
XR_002957959.1:n.816+130_816+131del
NM_198844.3:c.559+130_559+131del	NP_942141.2:n.559+130_559+131del
NM_199321.3:c.625+130_625+131del MANE Select	NP_955353.1:n.625+130_625+131del