Canonical Allele Identifier: CA8535973

Gene: ZPBP2

Linked Data

• dbSNP Id: rs778676815
• ExAC: 17:38028636 C / CT
• gnomAD v2: 17-38028636-C-CT
• gnomAD v3: 17-39872383-C-CT
• gnomAD v4: 17-39872383-C-CT
• MyVariant Identifiers: chr17:g.38028636_38028637insT (hg19) ; chr17:g.39872383_39872384insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872384dup , CM000679.2:g.39872384dup	GRCh38
NC_000017.10:g.38028637dup , CM000679.1:g.38028637dup	GRCh37
NC_000017.9:g.35282163dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000348931.9:c.521dup MANE Select	ENSP00000335384.5:p.Ile175AsnfsTer3
ENST00000348931.8:c.521dup	ENSP00000335384.5:p.Ile175AsnfsTer3
ENST00000377940.3:c.455dup	ENSP00000367174.3:p.Ile153AsnfsTer3
ENST00000583811.5:c.167dup	ENSP00000462463.1:p.Ile57AsnfsTer3
ENST00000584588.5:c.407-660dup	ENSP00000462067.1:n.407-660dup
NM_198844.2:c.455dup	NP_942141.2:p.Ile153AsnfsTer3
NM_199321.2:c.521dup	NP_955353.1:p.Ile175AsnfsTer3
XM_011524298.1:c.521dup	XP_011522600.1:p.Ile175AsnfsTer3
XR_002957959.1:n.712dup
NM_198844.3:c.455dup	NP_942141.2:p.Ile153AsnfsTer3
NM_199321.3:c.521dup MANE Select	NP_955353.1:p.Ile175AsnfsTer3