Canonical Allele Identifier: CA290453431

Gene: ZPBP2

Linked Data

• dbSNP Id: rs756399122
• gnomAD v2: 17-38025343-A-AT
• gnomAD v3: 17-39869090-A-AT
• gnomAD v4: 17-39869090-A-AT
• MyVariant Identifiers: chr17:g.38025343_38025344insT (hg19) ; chr17:g.39869090_39869091insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39869091dup , CM000679.2:g.39869091dup	GRCh38
NC_000017.10:g.38025344dup , CM000679.1:g.38025344dup	GRCh37
NC_000017.9:g.35278870dup	NCBI36
NG_029104.2:g.98dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000348931.9:c.118+477dup MANE Select	ENSP00000335384.5:n.118+477dup
ENST00000348931.8:c.118+477dup	ENSP00000335384.5:n.118+477dup
ENST00000377940.3:c.52+685dup	ENSP00000367174.3:n.52+685dup
ENST00000583811.5:c.52+685dup	ENSP00000462463.1:n.52+685dup
ENST00000584588.5:c.118+477dup	ENSP00000462067.1:n.118+477dup
NM_198844.2:c.52+685dup	NP_942141.2:n.52+685dup
NM_199321.2:c.118+477dup	NP_955353.1:n.118+477dup
XM_011524298.1:c.118+477dup	XP_011522600.1:n.118+477dup
XR_002957959.1:n.309+477dup
NM_198844.3:c.52+685dup	NP_942141.2:n.52+685dup
NM_199321.3:c.118+477dup MANE Select	NP_955353.1:n.118+477dup