Canonical Allele Identifier: CA983635402

Gene: ZPBP2

Linked Data

• dbSNP Id: rs2063370541
• gnomAD v3: 17-39872593-ATGTT-A
• gnomAD v4: 17-39872593-ATGTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872598_39872601del , CM000679.2:g.39872598_39872601del	GRCh38
NC_000017.10:g.38028851_38028854del , CM000679.1:g.38028851_38028854del	GRCh37
NC_000017.9:g.35282377_35282380del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.625+110_625+113del MANE Select	ENSP00000335384.5:n.625+110_625+113del
ENST00000348931.8:c.625+110_625+113del	ENSP00000335384.5:n.625+110_625+113del
ENST00000377940.3:c.559+110_559+113del	ENSP00000367174.3:n.559+110_559+113del
ENST00000583811.5:c.271+110_271+113del	ENSP00000462463.1:n.271+110_271+113del
ENST00000584588.5:c.407-446_407-443del	ENSP00000462067.1:n.407-446_407-443del
NM_198844.2:c.559+110_559+113del	NP_942141.2:n.559+110_559+113del
NM_199321.2:c.625+110_625+113del	NP_955353.1:n.625+110_625+113del
XM_011524298.1:c.625+110_625+113del	XP_011522600.1:n.625+110_625+113del
XR_002957959.1:n.816+110_816+113del
NM_198844.3:c.559+110_559+113del	NP_942141.2:n.559+110_559+113del
NM_199321.3:c.625+110_625+113del MANE Select	NP_955353.1:n.625+110_625+113del