Canonical Allele Identifier: CA645539568

Gene: POGZ

Linked Data

• COSMIC: COSM4716360 ; COSM4716361

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151424963del , CM000663.2:g.151424963del	GRCh38
NC_000001.10:g.151397439del , CM000663.1:g.151397439del	GRCh37
NC_000001.9:g.149664063del	NCBI36
NG_046601.1:g.39503del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.1225del	ENSP00000518163.1:p.His409ThrfsTer?
ENST00000392723.6:c.1018del	ENSP00000376484.1:p.His340ThrfsTer?
ENST00000439756.2:c.1177del	ENSP00000390156.2:p.His393ThrfsTer?
ENST00000703168.1:c.1198del	ENSP00000515214.1:p.His400ThrfsTer?
ENST00000703169.1:c.1150del	ENSP00000515215.1:p.His384ThrfsTer?
ENST00000271715.7:c.1177del MANE Select	ENSP00000271715.2:p.His393ThrfsTer?
ENST00000271715.6:c.1177del	ENSP00000271715.2:p.His393ThrfsTer?
ENST00000358476.7:n.1046del
ENST00000368863.6:c.892del	ENSP00000357856.2:p.His298ThrfsTer?
ENST00000392723.5:c.1018del	ENSP00000376484.1:p.His340ThrfsTer?
ENST00000409503.5:c.1150del	ENSP00000386836.1:p.His384ThrfsTer?
ENST00000441516.1:c.159-677del
ENST00000491586.5:c.1018del	ENSP00000418408.1:p.His340ThrfsTer?
ENST00000495253.1:n.332del
ENST00000531094.5:c.991del	ENSP00000431259.1:p.His331ThrfsTer?
NM_001194937.1:c.1150del	NP_001181866.1:p.His384ThrfsTer?
NM_001194938.1:c.991del	NP_001181867.1:p.His331ThrfsTer?
NM_015100.3:c.1177del	NP_055915.2:p.His393ThrfsTer?
NM_145796.3:c.892del	NP_665739.3:p.His298ThrfsTer?
NM_207171.2:c.1018del	NP_997054.1:p.His340ThrfsTer?
XM_005244999.1:c.1177del	XP_005245056.1:p.His393ThrfsTer?
XM_005245000.3:c.1177del	XP_005245057.1:p.His393ThrfsTer?
XM_005245001.1:c.1177del	XP_005245058.1:p.His393ThrfsTer?
XM_005245005.1:c.1018del	XP_005245062.1:p.His340ThrfsTer?
XM_005245006.3:c.1018del	XP_005245063.1:p.His340ThrfsTer?
XM_011509330.1:c.1069del	XP_011507632.1:p.His357ThrfsTer?
XM_011509331.1:c.820del	XP_011507633.1:p.His274ThrfsTer?
XR_921760.1:n.1178del
XM_005244999.3:c.1177del	XP_005245056.1:p.His393ThrfsTer?
XM_005245000.4:c.1177del	XP_005245057.1:p.His393ThrfsTer?
XM_005245001.2:c.1177del	XP_005245058.1:p.His393ThrfsTer?
XM_005245005.2:c.1018del	XP_005245062.1:p.His340ThrfsTer?
XM_005245006.5:c.1018del	XP_005245063.1:p.His340ThrfsTer?
XM_017000744.1:c.1198del	XP_016856233.1:p.His400ThrfsTer?
XM_017000745.2:c.1150del	XP_016856234.1:p.His384ThrfsTer?
XM_017000746.1:c.1150del	XP_016856235.1:p.His384ThrfsTer?
XM_017000748.1:c.1018del	XP_016856237.1:p.His340ThrfsTer?
XM_017000749.1:c.1018del	XP_016856238.1:p.His340ThrfsTer?
XM_024454305.1:c.1198del	XP_024310073.1:p.His400ThrfsTer?
XM_024454306.1:c.-15-677del	XP_024310074.1:n.-15-677del
XR_002959801.1:n.1205del
NM_015100.4:c.1177del MANE Select	NP_055915.2:p.His393ThrfsTer?
NM_001194937.2:c.1150del	NP_001181866.1:p.His384ThrfsTer?
NM_001194938.2:c.991del	NP_001181867.1:p.His331ThrfsTer?
NM_145796.4:c.892del	NP_665739.3:p.His298ThrfsTer?