Canonical Allele Identifier: CA2479570579

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406263_151406264delinsCG , CM000663.2:g.151406263_151406264delinsCG	GRCh38
NC_000001.10:g.151378739_151378740delinsCG , CM000663.1:g.151378739_151378740delinsCG	GRCh37
NC_000001.9:g.149645363_149645364delinsCG	NCBI36
NG_046601.1:g.58202_58203delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2819_2820delinsCG	ENSP00000518163.1:p.Pro940=
ENST00000392723.6:c.2612_2613delinsCG	ENSP00000376484.1:p.Pro871=
ENST00000439756.2:c.2771_2772delinsCG	ENSP00000390156.2:p.Pro924=
ENST00000703168.1:c.2792_2793delinsCG	ENSP00000515214.1:p.Pro931=
ENST00000271715.7:c.2771_2772delinsCG MANE Select	ENSP00000271715.2:p.Pro924=
ENST00000271715.6:c.2771_2772delinsCG	ENSP00000271715.2:p.Pro924=
ENST00000358476.7:n.2919_2920delinsCG
ENST00000368863.6:c.2486_2487delinsCG	ENSP00000357856.2:p.Pro829=
ENST00000392723.5:c.2612_2613delinsCG	ENSP00000376484.1:p.Pro871=
ENST00000409503.5:c.2744_2745delinsCG	ENSP00000386836.1:p.Pro915=
ENST00000491586.5:c.2639_2640delinsCG	ENSP00000418408.1:p.Pro880=
ENST00000531094.5:c.2585_2586delinsCG	ENSP00000431259.1:p.Pro862=
NM_001194937.1:c.2744_2745delinsCG	NP_001181866.1:p.Pro915=
NM_001194938.1:c.2585_2586delinsCG	NP_001181867.1:p.Pro862=
NM_015100.3:c.2771_2772delinsCG	NP_055915.2:p.Pro924=
NM_145796.3:c.2486_2487delinsCG	NP_665739.3:p.Pro829=
NM_207171.2:c.2612_2613delinsCG	NP_997054.1:p.Pro871=
XM_005244999.1:c.2771_2772delinsCG	XP_005245056.1:p.Pro924=
XM_005245000.3:c.2771_2772delinsCG	XP_005245057.1:p.Pro924=
XM_005245001.1:c.2771_2772delinsCG	XP_005245058.1:p.Pro924=
XM_005245005.1:c.2612_2613delinsCG	XP_005245062.1:p.Pro871=
XM_005245006.3:c.2612_2613delinsCG	XP_005245063.1:p.Pro871=
XM_011509330.1:c.2663_2664delinsCG	XP_011507632.1:p.Pro888=
XM_011509331.1:c.2414_2415delinsCG	XP_011507633.1:p.Pro805=
XM_005244999.3:c.2771_2772delinsCG	XP_005245056.1:p.Pro924=
XM_005245000.4:c.2771_2772delinsCG	XP_005245057.1:p.Pro924=
XM_005245001.2:c.2771_2772delinsCG	XP_005245058.1:p.Pro924=
XM_005245005.2:c.2612_2613delinsCG	XP_005245062.1:p.Pro871=
XM_005245006.5:c.2612_2613delinsCG	XP_005245063.1:p.Pro871=
XM_017000744.1:c.2792_2793delinsCG	XP_016856233.1:p.Pro931=
XM_017000745.2:c.2744_2745delinsCG	XP_016856234.1:p.Pro915=
XM_017000746.1:c.2744_2745delinsCG	XP_016856235.1:p.Pro915=
XM_017000748.1:c.2612_2613delinsCG	XP_016856237.1:p.Pro871=
XM_017000749.1:c.2612_2613delinsCG	XP_016856238.1:p.Pro871=
XM_024454305.1:c.2645_2646delinsCG	XP_024310073.1:p.Pro882=
XM_024454306.1:c.1571_1572delinsCG	XP_024310074.1:p.Pro524=
XR_002959801.1:n.2626_2627delinsCG
NM_015100.4:c.2771_2772delinsCG MANE Select	NP_055915.2:p.Pro924=
NM_001194937.2:c.2744_2745delinsCG	NP_001181866.1:p.Pro915=
NM_001194938.2:c.2585_2586delinsCG	NP_001181867.1:p.Pro862=
NM_145796.4:c.2486_2487delinsCG	NP_665739.3:p.Pro829=