Canonical Allele Identifier: CA2479570676

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406460_151406461delinsCA , CM000663.2:g.151406460_151406461delinsCA	GRCh38
NC_000001.10:g.151378936_151378937delinsCA , CM000663.1:g.151378936_151378937delinsCA	GRCh37
NC_000001.9:g.149645560_149645561delinsCA	NCBI36
NG_046601.1:g.58005_58006delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2622_2623delinsTG	ENSP00000518163.1:p.His874=
ENST00000392723.6:c.2415_2416delinsTG	ENSP00000376484.1:p.His805=
ENST00000439756.2:c.2574_2575delinsTG	ENSP00000390156.2:p.His858=
ENST00000703168.1:c.2595_2596delinsTG	ENSP00000515214.1:p.His865=
ENST00000271715.7:c.2574_2575delinsTG MANE Select	ENSP00000271715.2:p.His858=
ENST00000271715.6:c.2574_2575delinsTG	ENSP00000271715.2:p.His858=
ENST00000358476.7:n.2722_2723delinsTG
ENST00000368863.6:c.2289_2290delinsTG	ENSP00000357856.2:p.His763=
ENST00000392723.5:c.2415_2416delinsTG	ENSP00000376484.1:p.His805=
ENST00000409503.5:c.2547_2548delinsTG	ENSP00000386836.1:p.His849=
ENST00000491586.5:c.2442_2443delinsTG	ENSP00000418408.1:p.His814=
ENST00000529669.1:c.774_775delinsTG	ENSP00000432295.1:p.His258=
ENST00000531094.5:c.2388_2389delinsTG	ENSP00000431259.1:p.His796=
NM_001194937.1:c.2547_2548delinsTG	NP_001181866.1:p.His849=
NM_001194938.1:c.2388_2389delinsTG	NP_001181867.1:p.His796=
NM_015100.3:c.2574_2575delinsTG	NP_055915.2:p.His858=
NM_145796.3:c.2289_2290delinsTG	NP_665739.3:p.His763=
NM_207171.2:c.2415_2416delinsTG	NP_997054.1:p.His805=
XM_005244999.1:c.2574_2575delinsTG	XP_005245056.1:p.His858=
XM_005245000.3:c.2574_2575delinsTG	XP_005245057.1:p.His858=
XM_005245001.1:c.2574_2575delinsTG	XP_005245058.1:p.His858=
XM_005245005.1:c.2415_2416delinsTG	XP_005245062.1:p.His805=
XM_005245006.3:c.2415_2416delinsTG	XP_005245063.1:p.His805=
XM_011509330.1:c.2466_2467delinsTG	XP_011507632.1:p.His822=
XM_011509331.1:c.2217_2218delinsTG	XP_011507633.1:p.His739=
XR_921760.1:n.2402_2403delinsTG
XM_005244999.3:c.2574_2575delinsTG	XP_005245056.1:p.His858=
XM_005245000.4:c.2574_2575delinsTG	XP_005245057.1:p.His858=
XM_005245001.2:c.2574_2575delinsTG	XP_005245058.1:p.His858=
XM_005245005.2:c.2415_2416delinsTG	XP_005245062.1:p.His805=
XM_005245006.5:c.2415_2416delinsTG	XP_005245063.1:p.His805=
XM_017000744.1:c.2595_2596delinsTG	XP_016856233.1:p.His865=
XM_017000745.2:c.2547_2548delinsTG	XP_016856234.1:p.His849=
XM_017000746.1:c.2547_2548delinsTG	XP_016856235.1:p.His849=
XM_017000748.1:c.2415_2416delinsTG	XP_016856237.1:p.His805=
XM_017000749.1:c.2415_2416delinsTG	XP_016856238.1:p.His805=
XM_024454305.1:c.2448_2449delinsTG	XP_024310073.1:p.His816=
XM_024454306.1:c.1374_1375delinsTG	XP_024310074.1:p.His458=
XR_002959801.1:n.2429_2430delinsTG
NM_015100.4:c.2574_2575delinsTG MANE Select	NP_055915.2:p.His858=
NM_001194937.2:c.2547_2548delinsTG	NP_001181866.1:p.His849=
NM_001194938.2:c.2388_2389delinsTG	NP_001181867.1:p.His796=
NM_145796.4:c.2289_2290delinsTG	NP_665739.3:p.His763=