Canonical Allele Identifier: CA2843744582
Gene: POGZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151406047del , CM000663.2:g.151406047del GRCh38
NC_000001.10:g.151378523del , CM000663.1:g.151378523del GRCh37
NC_000001.9:g.149645147del NCBI36
NG_046601.1:g.58420del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710270.1:c.3037del ENSP00000518163.1:p.Arg1013GlufsTer22
ENST00000392723.6:c.2830del ENSP00000376484.1:p.Arg944GlufsTer22
ENST00000439756.2:c.2989del ENSP00000390156.2:p.Arg997GlufsTer22
ENST00000703168.1:c.3010del ENSP00000515214.1:p.Arg1004GlufsTer22
ENST00000271715.7:c.2989del MANE Select ENSP00000271715.2:p.Arg997GlufsTer22
ENST00000271715.6:c.2989del ENSP00000271715.2:p.Arg997GlufsTer22
ENST00000358476.7:n.3137del
ENST00000368863.6:c.2704del ENSP00000357856.2:p.Arg902GlufsTer22
ENST00000392723.5:c.2830del ENSP00000376484.1:p.Arg944GlufsTer22
ENST00000409503.5:c.2962del ENSP00000386836.1:p.Arg988GlufsTer22
ENST00000491586.5:c.2857del ENSP00000418408.1:p.Arg953GlufsTer22
ENST00000531094.5:c.2803del ENSP00000431259.1:p.Arg935GlufsTer22
NM_001194937.1:c.2962del NP_001181866.1:p.Arg988GlufsTer22
NM_001194938.1:c.2803del NP_001181867.1:p.Arg935GlufsTer22
NM_015100.3:c.2989del NP_055915.2:p.Arg997GlufsTer22
NM_145796.3:c.2704del NP_665739.3:p.Arg902GlufsTer22
NM_207171.2:c.2830del NP_997054.1:p.Arg944GlufsTer22
XM_005244999.1:c.2989del XP_005245056.1:p.Arg997GlufsTer22
XM_005245000.3:c.2989del XP_005245057.1:p.Arg997GlufsTer22
XM_005245001.1:c.2989del XP_005245058.1:p.Arg997GlufsTer22
XM_005245005.1:c.2830del XP_005245062.1:p.Arg944GlufsTer22
XM_005245006.3:c.2830del XP_005245063.1:p.Arg944GlufsTer22
XM_011509330.1:c.2881del XP_011507632.1:p.Arg961GlufsTer22
XM_011509331.1:c.2632del XP_011507633.1:p.Arg878GlufsTer22
XM_005244999.3:c.2989del XP_005245056.1:p.Arg997GlufsTer22
XM_005245000.4:c.2989del XP_005245057.1:p.Arg997GlufsTer22
XM_005245001.2:c.2989del XP_005245058.1:p.Arg997GlufsTer22
XM_005245005.2:c.2830del XP_005245062.1:p.Arg944GlufsTer22
XM_005245006.5:c.2830del XP_005245063.1:p.Arg944GlufsTer22
XM_017000744.1:c.3010del XP_016856233.1:p.Arg1004GlufsTer22
XM_017000745.2:c.2962del XP_016856234.1:p.Arg988GlufsTer22
XM_017000746.1:c.2962del XP_016856235.1:p.Arg988GlufsTer22
XM_017000748.1:c.2830del XP_016856237.1:p.Arg944GlufsTer22
XM_017000749.1:c.2830del XP_016856238.1:p.Arg944GlufsTer22
XM_024454305.1:c.2863del XP_024310073.1:p.Arg955GlufsTer22
XM_024454306.1:c.1789del XP_024310074.1:p.Arg597GlufsTer22
XR_002959801.1:n.2844del
NM_015100.4:c.2989del MANE Select NP_055915.2:p.Arg997GlufsTer22
NM_001194937.2:c.2962del NP_001181866.1:p.Arg988GlufsTer22
NM_001194938.2:c.2803del NP_001181867.1:p.Arg935GlufsTer22
NM_145796.4:c.2704del NP_665739.3:p.Arg902GlufsTer22