Canonical Allele Identifier: CA4260870

Gene: ZPBP

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.50081848G>A , CM000669.2:g.50081848G>A	GRCh38
NC_000007.13:g.50121444G>A , CM000669.1:g.50121444G>A	GRCh37
NC_000007.12:g.50091990G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000046087.7:c.260C>T MANE Select	ENSP00000046087.2:p.Thr87Met
ENST00000046087.6:c.260C>T	ENSP00000046087.2:p.Thr87Met
ENST00000419417.5:c.260C>T	ENSP00000402071.1:p.Thr87Met
ENST00000450231.1:c.143C>T	ENSP00000390054.1:p.Thr48Met
NM_001159878.1:c.260C>T	NP_001153350.1:p.Thr87Met
NM_007009.2:c.260C>T	NP_008940.2:p.Thr87Met
XM_011515095.1:c.260C>T	XP_011513397.1:p.Thr87Met
XM_011515096.1:c.260C>T	XP_011513398.1:p.Thr87Met
XM_011515097.1:c.260C>T	XP_011513399.1:p.Thr87Met
XM_011515098.1:c.260C>T	XP_011513400.1:p.Thr87Met
XM_011515099.1:c.260C>T	XP_011513401.1:p.Thr87Met
XM_011515100.1:c.208+7781C>T	XP_011513402.1:n.208+7781C>T
XM_011515101.1:c.260C>T	XP_011513403.1:p.Thr87Met
XM_011515102.1:c.38C>T	XP_011513404.1:p.Thr13Met
XM_011515103.1:c.260C>T	XP_011513405.1:p.Thr87Met
XM_011515095.2:c.260C>T	XP_011513397.1:p.Thr87Met
XM_011515096.2:c.260C>T	XP_011513398.1:p.Thr87Met
XM_011515100.2:c.208+7781C>T	XP_011513402.1:n.208+7781C>T
XM_011515101.3:c.260C>T	XP_011513403.1:p.Thr87Met
XM_011515102.2:c.38C>T	XP_011513404.1:p.Thr13Met
XM_017011707.1:c.260C>T	XP_016867196.1:p.Thr87Met
XM_024446645.1:c.260C>T	XP_024302413.1:p.Thr87Met
XM_024446646.1:c.38C>T	XP_024302414.1:p.Thr13Met
XR_001744543.1:n.324C>T
NM_007009.3:c.260C>T MANE Select	NP_008940.2:p.Thr87Met
NM_001159878.2:c.260C>T	NP_001153350.1:p.Thr87Met