Canonical Allele Identifier: CA2259291025

Gene: ZPBP2

Linked Data

• dbSNP Id: rs2063371123

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872734_39872737del , CM000679.2:g.39872734_39872737del	GRCh38
NC_000017.10:g.38028987_38028990del , CM000679.1:g.38028987_38028990del	GRCh37
NC_000017.9:g.35282513_35282516del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.625+246_625+249del MANE Select	ENSP00000335384.5:n.625+246_625+249del
ENST00000348931.8:c.625+246_625+249del	ENSP00000335384.5:n.625+246_625+249del
ENST00000377940.3:c.559+246_559+249del	ENSP00000367174.3:n.559+246_559+249del
ENST00000583811.5:c.271+246_271+249del	ENSP00000462463.1:n.271+246_271+249del
ENST00000584588.5:c.407-310_407-307del	ENSP00000462067.1:n.407-310_407-307del
NM_198844.2:c.559+246_559+249del	NP_942141.2:n.559+246_559+249del
NM_199321.2:c.625+246_625+249del	NP_955353.1:n.625+246_625+249del
XM_011524298.1:c.625+246_625+249del	XP_011522600.1:n.625+246_625+249del
XR_002957959.1:n.816+246_816+249del
NM_198844.3:c.559+246_559+249del	NP_942141.2:n.559+246_559+249del
NM_199321.3:c.625+246_625+249del MANE Select	NP_955353.1:n.625+246_625+249del