Canonical Allele Identifier: CA2586967478

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151424959_151424962delinsGG , CM000663.2:g.151424959_151424962delinsGG	GRCh38
NC_000001.10:g.151397435_151397438delinsGG , CM000663.1:g.151397435_151397438delinsGG	GRCh37
NC_000001.9:g.149664059_149664062delinsGG	NCBI36
NG_046601.1:g.39504_39507delinsCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.1226_1229delinsCC	ENSP00000518163.1:p.His409ProfsTer10
ENST00000392723.6:c.1019_1022delinsCC	ENSP00000376484.1:p.His340ProfsTer10
ENST00000439756.2:c.1178_1181delinsCC	ENSP00000390156.2:p.His393ProfsTer10
ENST00000703168.1:c.1199_1202delinsCC	ENSP00000515214.1:p.His400ProfsTer10
ENST00000703169.1:c.1151_1154delinsCC	ENSP00000515215.1:p.His384ProfsTer10
ENST00000271715.7:c.1178_1181delinsCC MANE Select	ENSP00000271715.2:p.His393ProfsTer10
ENST00000271715.6:c.1178_1181delinsCC	ENSP00000271715.2:p.His393ProfsTer10
ENST00000358476.7:n.1047_1050delinsCC
ENST00000368863.6:c.893_896delinsCC	ENSP00000357856.2:p.His298ProfsTer10
ENST00000392723.5:c.1019_1022delinsCC	ENSP00000376484.1:p.His340ProfsTer10
ENST00000409503.5:c.1151_1154delinsCC	ENSP00000386836.1:p.His384ProfsTer10
ENST00000441516.1:c.159-676_159-673delinsCC
ENST00000491586.5:c.1019_1022delinsCC	ENSP00000418408.1:p.His340ProfsTer10
ENST00000495253.1:n.333_336delinsCC
ENST00000531094.5:c.992_995delinsCC	ENSP00000431259.1:p.His331ProfsTer10
NM_001194937.1:c.1151_1154delinsCC	NP_001181866.1:p.His384ProfsTer10
NM_001194938.1:c.992_995delinsCC	NP_001181867.1:p.His331ProfsTer10
NM_015100.3:c.1178_1181delinsCC	NP_055915.2:p.His393ProfsTer10
NM_145796.3:c.893_896delinsCC	NP_665739.3:p.His298ProfsTer10
NM_207171.2:c.1019_1022delinsCC	NP_997054.1:p.His340ProfsTer10
XM_005244999.1:c.1178_1181delinsCC	XP_005245056.1:p.His393ProfsTer10
XM_005245000.3:c.1178_1181delinsCC	XP_005245057.1:p.His393ProfsTer10
XM_005245001.1:c.1178_1181delinsCC	XP_005245058.1:p.His393ProfsTer10
XM_005245005.1:c.1019_1022delinsCC	XP_005245062.1:p.His340ProfsTer10
XM_005245006.3:c.1019_1022delinsCC	XP_005245063.1:p.His340ProfsTer10
XM_011509330.1:c.1070_1073delinsCC	XP_011507632.1:p.His357ProfsTer10
XM_011509331.1:c.821_824delinsCC	XP_011507633.1:p.His274ProfsTer10
XR_921760.1:n.1179_1182delinsCC
XM_005244999.3:c.1178_1181delinsCC	XP_005245056.1:p.His393ProfsTer10
XM_005245000.4:c.1178_1181delinsCC	XP_005245057.1:p.His393ProfsTer10
XM_005245001.2:c.1178_1181delinsCC	XP_005245058.1:p.His393ProfsTer10
XM_005245005.2:c.1019_1022delinsCC	XP_005245062.1:p.His340ProfsTer10
XM_005245006.5:c.1019_1022delinsCC	XP_005245063.1:p.His340ProfsTer10
XM_017000744.1:c.1199_1202delinsCC	XP_016856233.1:p.His400ProfsTer10
XM_017000745.2:c.1151_1154delinsCC	XP_016856234.1:p.His384ProfsTer10
XM_017000746.1:c.1151_1154delinsCC	XP_016856235.1:p.His384ProfsTer10
XM_017000748.1:c.1019_1022delinsCC	XP_016856237.1:p.His340ProfsTer10
XM_017000749.1:c.1019_1022delinsCC	XP_016856238.1:p.His340ProfsTer10
XM_024454305.1:c.1199_1202delinsCC	XP_024310073.1:p.His400ProfsTer10
XM_024454306.1:c.-15-676_-15-673delinsCC	XP_024310074.1:n.-15-676_-15-673delinsCC
XR_002959801.1:n.1206_1209delinsCC
NM_015100.4:c.1178_1181delinsCC MANE Select	NP_055915.2:p.His393ProfsTer10
NM_001194937.2:c.1151_1154delinsCC	NP_001181866.1:p.His384ProfsTer10
NM_001194938.2:c.992_995delinsCC	NP_001181867.1:p.His331ProfsTer10
NM_145796.4:c.893_896delinsCC	NP_665739.3:p.His298ProfsTer10