Canonical Allele Identifier: CA2259291019
Gene: ZPBP2 HGNC NCBI

Linked Data

dbSNP Id: rs2063371081

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872711_39872715del , CM000679.2:g.39872711_39872715del GRCh38
NC_000017.10:g.38028964_38028968del , CM000679.1:g.38028964_38028968del GRCh37
NC_000017.9:g.35282490_35282494del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.625+223_625+227del MANE Select ENSP00000335384.5:n.625+223_625+227del
ENST00000348931.8:c.625+223_625+227del ENSP00000335384.5:n.625+223_625+227del
ENST00000377940.3:c.559+223_559+227del ENSP00000367174.3:n.559+223_559+227del
ENST00000583811.5:c.271+223_271+227del ENSP00000462463.1:n.271+223_271+227del
ENST00000584588.5:c.407-333_407-329del ENSP00000462067.1:n.407-333_407-329del
NM_198844.2:c.559+223_559+227del NP_942141.2:n.559+223_559+227del
NM_199321.2:c.625+223_625+227del NP_955353.1:n.625+223_625+227del
XM_011524298.1:c.625+223_625+227del XP_011522600.1:n.625+223_625+227del
XR_002957959.1:n.816+223_816+227del
NM_198844.3:c.559+223_559+227del NP_942141.2:n.559+223_559+227del
NM_199321.3:c.625+223_625+227del MANE Select NP_955353.1:n.625+223_625+227del