Canonical Allele Identifier: CA2557817760

Gene: ZPBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872498_39872500del , CM000679.2:g.39872498_39872500del	GRCh38
NC_000017.10:g.38028751_38028753del , CM000679.1:g.38028751_38028753del	GRCh37
NC_000017.9:g.35282277_35282279del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.625+10_625+12del MANE Select	ENSP00000335384.5:n.625+10_625+12del
ENST00000348931.8:c.625+10_625+12del	ENSP00000335384.5:n.625+10_625+12del
ENST00000377940.3:c.559+10_559+12del	ENSP00000367174.3:n.559+10_559+12del
ENST00000583811.5:c.271+10_271+12del	ENSP00000462463.1:n.271+10_271+12del
ENST00000584588.5:c.407-546_407-544del	ENSP00000462067.1:n.407-546_407-544del
NM_198844.2:c.559+10_559+12del	NP_942141.2:n.559+10_559+12del
NM_199321.2:c.625+10_625+12del	NP_955353.1:n.625+10_625+12del
XM_011524298.1:c.625+10_625+12del	XP_011522600.1:n.625+10_625+12del
XR_002957959.1:n.816+10_816+12del
NM_198844.3:c.559+10_559+12del	NP_942141.2:n.559+10_559+12del
NM_199321.3:c.625+10_625+12del MANE Select	NP_955353.1:n.625+10_625+12del