Canonical Allele Identifier: CA771905979

Gene: ZPBP2

Linked Data

• dbSNP Id: rs1257009657
• gnomAD v3: 17-39872143-TTA-T
• gnomAD v4: 17-39872143-TTA-T
• MyVariant Identifiers: chr17:g.38028397_38028398del (hg19) ; chr17:g.39872144_39872145del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872145_39872146del , CM000679.2:g.39872145_39872146del	GRCh38
NC_000017.10:g.38028398_38028399del , CM000679.1:g.38028398_38028399del	GRCh37
NC_000017.9:g.35281924_35281925del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.407-125_407-124del MANE Select	ENSP00000335384.5:n.407-125_407-124del
ENST00000348931.8:c.407-125_407-124del	ENSP00000335384.5:n.407-125_407-124del
ENST00000377940.3:c.341-125_341-124del	ENSP00000367174.3:n.341-125_341-124del
ENST00000583811.5:c.53-125_53-124del	ENSP00000462463.1:n.53-125_53-124del
ENST00000584588.5:c.406+520_406+521del	ENSP00000462067.1:n.406+520_406+521del
NM_198844.2:c.341-125_341-124del	NP_942141.2:n.341-125_341-124del
NM_199321.2:c.407-125_407-124del	NP_955353.1:n.407-125_407-124del
XM_011524298.1:c.407-125_407-124del	XP_011522600.1:n.407-125_407-124del
XR_002957959.1:n.598-125_598-124del
NM_198844.3:c.341-125_341-124del	NP_942141.2:n.341-125_341-124del
NM_199321.3:c.407-125_407-124del MANE Select	NP_955353.1:n.407-125_407-124del