Canonical Allele Identifier: CA625946604

Gene: ZPBP2

Linked Data

• dbSNP Id: rs1374243738
• gnomAD v2: 17-38028953-AAATC-A
• gnomAD v3: 17-39872700-AAATC-A
• gnomAD v4: 17-39872700-AAATC-A
• MyVariant Identifiers: chr17:g.38028954_38028957del (hg19) ; chr17:g.39872701_39872704del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872704_39872707del , CM000679.2:g.39872704_39872707del	GRCh38
NC_000017.10:g.38028957_38028960del , CM000679.1:g.38028957_38028960del	GRCh37
NC_000017.9:g.35282483_35282486del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.625+216_625+219del MANE Select	ENSP00000335384.5:n.625+216_625+219del
ENST00000348931.8:c.625+216_625+219del	ENSP00000335384.5:n.625+216_625+219del
ENST00000377940.3:c.559+216_559+219del	ENSP00000367174.3:n.559+216_559+219del
ENST00000583811.5:c.271+216_271+219del	ENSP00000462463.1:n.271+216_271+219del
ENST00000584588.5:c.407-340_407-337del	ENSP00000462067.1:n.407-340_407-337del
NM_198844.2:c.559+216_559+219del	NP_942141.2:n.559+216_559+219del
NM_199321.2:c.625+216_625+219del	NP_955353.1:n.625+216_625+219del
XM_011524298.1:c.625+216_625+219del	XP_011522600.1:n.625+216_625+219del
XR_002957959.1:n.816+216_816+219del
NM_198844.3:c.559+216_559+219del	NP_942141.2:n.559+216_559+219del
NM_199321.3:c.625+216_625+219del MANE Select	NP_955353.1:n.625+216_625+219del