Canonical Allele Identifier: CA2479570669
Gene: POGZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151406444C= , CM000663.2:g.151406444C= GRCh38
NC_000001.10:g.151378920C= , CM000663.1:g.151378920C= GRCh37
NC_000001.9:g.149645544C= NCBI36
NG_046601.1:g.58022G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710270.1:c.2639G= ENSP00000518163.1:p.Arg880=
ENST00000392723.6:c.2432G= ENSP00000376484.1:p.Arg811=
ENST00000439756.2:c.2591G= ENSP00000390156.2:p.Arg864=
ENST00000703168.1:c.2612G= ENSP00000515214.1:p.Arg871=
ENST00000271715.7:c.2591G= MANE Select ENSP00000271715.2:p.Arg864=
ENST00000271715.6:c.2591G= ENSP00000271715.2:p.Arg864=
ENST00000358476.7:n.2739G=
ENST00000368863.6:c.2306G= ENSP00000357856.2:p.Arg769=
ENST00000392723.5:c.2432G= ENSP00000376484.1:p.Arg811=
ENST00000409503.5:c.2564G= ENSP00000386836.1:p.Arg855=
ENST00000491586.5:c.2459G= ENSP00000418408.1:p.Arg820=
ENST00000529669.1:c.791G= ENSP00000432295.1:p.Arg264=
ENST00000531094.5:c.2405G= ENSP00000431259.1:p.Arg802=
NM_001194937.1:c.2564G= NP_001181866.1:p.Arg855=
NM_001194938.1:c.2405G= NP_001181867.1:p.Arg802=
NM_015100.3:c.2591G= NP_055915.2:p.Arg864=
NM_145796.3:c.2306G= NP_665739.3:p.Arg769=
NM_207171.2:c.2432G= NP_997054.1:p.Arg811=
XM_005244999.1:c.2591G= XP_005245056.1:p.Arg864=
XM_005245000.3:c.2591G= XP_005245057.1:p.Arg864=
XM_005245001.1:c.2591G= XP_005245058.1:p.Arg864=
XM_005245005.1:c.2432G= XP_005245062.1:p.Arg811=
XM_005245006.3:c.2432G= XP_005245063.1:p.Arg811=
XM_011509330.1:c.2483G= XP_011507632.1:p.Arg828=
XM_011509331.1:c.2234G= XP_011507633.1:p.Arg745=
XR_921760.1:n.2419G=
XM_005244999.3:c.2591G= XP_005245056.1:p.Arg864=
XM_005245000.4:c.2591G= XP_005245057.1:p.Arg864=
XM_005245001.2:c.2591G= XP_005245058.1:p.Arg864=
XM_005245005.2:c.2432G= XP_005245062.1:p.Arg811=
XM_005245006.5:c.2432G= XP_005245063.1:p.Arg811=
XM_017000744.1:c.2612G= XP_016856233.1:p.Arg871=
XM_017000745.2:c.2564G= XP_016856234.1:p.Arg855=
XM_017000746.1:c.2564G= XP_016856235.1:p.Arg855=
XM_017000748.1:c.2432G= XP_016856237.1:p.Arg811=
XM_017000749.1:c.2432G= XP_016856238.1:p.Arg811=
XM_024454305.1:c.2465G= XP_024310073.1:p.Arg822=
XM_024454306.1:c.1391G= XP_024310074.1:p.Arg464=
XR_002959801.1:n.2446G=
NM_015100.4:c.2591G= MANE Select NP_055915.2:p.Arg864=
NM_001194937.2:c.2564G= NP_001181866.1:p.Arg855=
NM_001194938.2:c.2405G= NP_001181867.1:p.Arg802=
NM_145796.4:c.2306G= NP_665739.3:p.Arg769=