Canonical Allele Identifier: CA771905927
Gene: ZPBP2 HGNC NCBI

Linked Data

dbSNP Id: rs1319150493
MyVariant Identifiers: chr17:g.38028246del (hg19) chr17:g.39871993del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39871995del , CM000679.2:g.39871995del GRCh38
NC_000017.10:g.38028248del , CM000679.1:g.38028248del GRCh37
NC_000017.9:g.35281774del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.407-275del MANE Select ENSP00000335384.5:n.407-275del
ENST00000348931.8:c.407-275del ENSP00000335384.5:n.407-275del
ENST00000377940.3:c.341-275del ENSP00000367174.3:n.341-275del
ENST00000583811.5:c.53-275del ENSP00000462463.1:n.53-275del
ENST00000584588.5:c.406+370del ENSP00000462067.1:n.406+370del
NM_198844.2:c.341-275del NP_942141.2:n.341-275del
NM_199321.2:c.407-275del NP_955353.1:n.407-275del
XM_011524298.1:c.407-275del XP_011522600.1:n.407-275del
XR_002957959.1:n.598-275del
NM_198844.3:c.341-275del NP_942141.2:n.341-275del
NM_199321.3:c.407-275del MANE Select NP_955353.1:n.407-275del
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