Canonical Allele Identifier: CA2574056016

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406167_151406168insA , CM000663.2:g.151406167_151406168insA	GRCh38
NC_000001.10:g.151378643_151378644insA , CM000663.1:g.151378643_151378644insA	GRCh37
NC_000001.9:g.149645267_149645268insA	NCBI36
NG_046601.1:g.58298_58299insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2915_2916insT	ENSP00000518163.1:p.Glu972AspfsTer9
ENST00000392723.6:c.2708_2709insT	ENSP00000376484.1:p.Glu903AspfsTer9
ENST00000439756.2:c.2867_2868insT	ENSP00000390156.2:p.Glu956AspfsTer9
ENST00000703168.1:c.2888_2889insT	ENSP00000515214.1:p.Glu963AspfsTer9
ENST00000271715.7:c.2867_2868insT MANE Select	ENSP00000271715.2:p.Glu956AspfsTer9
ENST00000271715.6:c.2867_2868insT	ENSP00000271715.2:p.Glu956AspfsTer9
ENST00000358476.7:n.3015_3016insT
ENST00000368863.6:c.2582_2583insT	ENSP00000357856.2:p.Glu861AspfsTer9
ENST00000392723.5:c.2708_2709insT	ENSP00000376484.1:p.Glu903AspfsTer9
ENST00000409503.5:c.2840_2841insT	ENSP00000386836.1:p.Glu947AspfsTer9
ENST00000491586.5:c.2735_2736insT	ENSP00000418408.1:p.Glu912AspfsTer9
ENST00000531094.5:c.2681_2682insT	ENSP00000431259.1:p.Glu894AspfsTer9
NM_001194937.1:c.2840_2841insT	NP_001181866.1:p.Glu947AspfsTer9
NM_001194938.1:c.2681_2682insT	NP_001181867.1:p.Glu894AspfsTer9
NM_015100.3:c.2867_2868insT	NP_055915.2:p.Glu956AspfsTer9
NM_145796.3:c.2582_2583insT	NP_665739.3:p.Glu861AspfsTer9
NM_207171.2:c.2708_2709insT	NP_997054.1:p.Glu903AspfsTer9
XM_005244999.1:c.2867_2868insT	XP_005245056.1:p.Glu956AspfsTer9
XM_005245000.3:c.2867_2868insT	XP_005245057.1:p.Glu956AspfsTer9
XM_005245001.1:c.2867_2868insT	XP_005245058.1:p.Glu956AspfsTer9
XM_005245005.1:c.2708_2709insT	XP_005245062.1:p.Glu903AspfsTer9
XM_005245006.3:c.2708_2709insT	XP_005245063.1:p.Glu903AspfsTer9
XM_011509330.1:c.2759_2760insT	XP_011507632.1:p.Glu920AspfsTer9
XM_011509331.1:c.2510_2511insT	XP_011507633.1:p.Glu837AspfsTer9
XM_005244999.3:c.2867_2868insT	XP_005245056.1:p.Glu956AspfsTer9
XM_005245000.4:c.2867_2868insT	XP_005245057.1:p.Glu956AspfsTer9
XM_005245001.2:c.2867_2868insT	XP_005245058.1:p.Glu956AspfsTer9
XM_005245005.2:c.2708_2709insT	XP_005245062.1:p.Glu903AspfsTer9
XM_005245006.5:c.2708_2709insT	XP_005245063.1:p.Glu903AspfsTer9
XM_017000744.1:c.2888_2889insT	XP_016856233.1:p.Glu963AspfsTer9
XM_017000745.2:c.2840_2841insT	XP_016856234.1:p.Glu947AspfsTer9
XM_017000746.1:c.2840_2841insT	XP_016856235.1:p.Glu947AspfsTer9
XM_017000748.1:c.2708_2709insT	XP_016856237.1:p.Glu903AspfsTer9
XM_017000749.1:c.2708_2709insT	XP_016856238.1:p.Glu903AspfsTer9
XM_024454305.1:c.2741_2742insT	XP_024310073.1:p.Glu914AspfsTer9
XM_024454306.1:c.1667_1668insT	XP_024310074.1:p.Glu556AspfsTer9
XR_002959801.1:n.2722_2723insT
NM_015100.4:c.2867_2868insT MANE Select	NP_055915.2:p.Glu956AspfsTer9
NM_001194937.2:c.2840_2841insT	NP_001181866.1:p.Glu947AspfsTer9
NM_001194938.2:c.2681_2682insT	NP_001181867.1:p.Glu894AspfsTer9
NM_145796.4:c.2582_2583insT	NP_665739.3:p.Glu861AspfsTer9