Canonical Allele Identifier: CA2479570551

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406198_151406199delinsTC , CM000663.2:g.151406198_151406199delinsTC	GRCh38
NC_000001.10:g.151378674_151378675delinsTC , CM000663.1:g.151378674_151378675delinsTC	GRCh37
NC_000001.9:g.149645298_149645299delinsTC	NCBI36
NG_046601.1:g.58267_58268delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2884_2885delinsGA	ENSP00000518163.1:p.Asp962=
ENST00000392723.6:c.2677_2678delinsGA	ENSP00000376484.1:p.Asp893=
ENST00000439756.2:c.2836_2837delinsGA	ENSP00000390156.2:p.Asp946=
ENST00000703168.1:c.2857_2858delinsGA	ENSP00000515214.1:p.Asp953=
ENST00000271715.7:c.2836_2837delinsGA MANE Select	ENSP00000271715.2:p.Asp946=
ENST00000271715.6:c.2836_2837delinsGA	ENSP00000271715.2:p.Asp946=
ENST00000358476.7:n.2984_2985delinsGA
ENST00000368863.6:c.2551_2552delinsGA	ENSP00000357856.2:p.Asp851=
ENST00000392723.5:c.2677_2678delinsGA	ENSP00000376484.1:p.Asp893=
ENST00000409503.5:c.2809_2810delinsGA	ENSP00000386836.1:p.Asp937=
ENST00000491586.5:c.2704_2705delinsGA	ENSP00000418408.1:p.Asp902=
ENST00000531094.5:c.2650_2651delinsGA	ENSP00000431259.1:p.Asp884=
NM_001194937.1:c.2809_2810delinsGA	NP_001181866.1:p.Asp937=
NM_001194938.1:c.2650_2651delinsGA	NP_001181867.1:p.Asp884=
NM_015100.3:c.2836_2837delinsGA	NP_055915.2:p.Asp946=
NM_145796.3:c.2551_2552delinsGA	NP_665739.3:p.Asp851=
NM_207171.2:c.2677_2678delinsGA	NP_997054.1:p.Asp893=
XM_005244999.1:c.2836_2837delinsGA	XP_005245056.1:p.Asp946=
XM_005245000.3:c.2836_2837delinsGA	XP_005245057.1:p.Asp946=
XM_005245001.1:c.2836_2837delinsGA	XP_005245058.1:p.Asp946=
XM_005245005.1:c.2677_2678delinsGA	XP_005245062.1:p.Asp893=
XM_005245006.3:c.2677_2678delinsGA	XP_005245063.1:p.Asp893=
XM_011509330.1:c.2728_2729delinsGA	XP_011507632.1:p.Asp910=
XM_011509331.1:c.2479_2480delinsGA	XP_011507633.1:p.Asp827=
XM_005244999.3:c.2836_2837delinsGA	XP_005245056.1:p.Asp946=
XM_005245000.4:c.2836_2837delinsGA	XP_005245057.1:p.Asp946=
XM_005245001.2:c.2836_2837delinsGA	XP_005245058.1:p.Asp946=
XM_005245005.2:c.2677_2678delinsGA	XP_005245062.1:p.Asp893=
XM_005245006.5:c.2677_2678delinsGA	XP_005245063.1:p.Asp893=
XM_017000744.1:c.2857_2858delinsGA	XP_016856233.1:p.Asp953=
XM_017000745.2:c.2809_2810delinsGA	XP_016856234.1:p.Asp937=
XM_017000746.1:c.2809_2810delinsGA	XP_016856235.1:p.Asp937=
XM_017000748.1:c.2677_2678delinsGA	XP_016856237.1:p.Asp893=
XM_017000749.1:c.2677_2678delinsGA	XP_016856238.1:p.Asp893=
XM_024454305.1:c.2710_2711delinsGA	XP_024310073.1:p.Asp904=
XM_024454306.1:c.1636_1637delinsGA	XP_024310074.1:p.Asp546=
XR_002959801.1:n.2691_2692delinsGA
NM_015100.4:c.2836_2837delinsGA MANE Select	NP_055915.2:p.Asp946=
NM_001194937.2:c.2809_2810delinsGA	NP_001181866.1:p.Asp937=
NM_001194938.2:c.2650_2651delinsGA	NP_001181867.1:p.Asp884=
NM_145796.4:c.2551_2552delinsGA	NP_665739.3:p.Asp851=