Canonical Allele Identifier: CA2479570596
Gene: POGZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151406303G= , CM000663.2:g.151406303G= GRCh38
NC_000001.10:g.151378779G= , CM000663.1:g.151378779G= GRCh37
NC_000001.9:g.149645403G= NCBI36
NG_046601.1:g.58163C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710270.1:c.2780C= ENSP00000518163.1:p.Pro927=
ENST00000392723.6:c.2573C= ENSP00000376484.1:p.Pro858=
ENST00000439756.2:c.2732C= ENSP00000390156.2:p.Pro911=
ENST00000703168.1:c.2753C= ENSP00000515214.1:p.Pro918=
ENST00000271715.7:c.2732C= MANE Select ENSP00000271715.2:p.Pro911=
ENST00000271715.6:c.2732C= ENSP00000271715.2:p.Pro911=
ENST00000358476.7:n.2880C=
ENST00000368863.6:c.2447C= ENSP00000357856.2:p.Pro816=
ENST00000392723.5:c.2573C= ENSP00000376484.1:p.Pro858=
ENST00000409503.5:c.2705C= ENSP00000386836.1:p.Pro902=
ENST00000491586.5:c.2600C= ENSP00000418408.1:p.Pro867=
ENST00000529669.1:c.932C= ENSP00000432295.1:p.Pro311=
ENST00000531094.5:c.2546C= ENSP00000431259.1:p.Pro849=
NM_001194937.1:c.2705C= NP_001181866.1:p.Pro902=
NM_001194938.1:c.2546C= NP_001181867.1:p.Pro849=
NM_015100.3:c.2732C= NP_055915.2:p.Pro911=
NM_145796.3:c.2447C= NP_665739.3:p.Pro816=
NM_207171.2:c.2573C= NP_997054.1:p.Pro858=
XM_005244999.1:c.2732C= XP_005245056.1:p.Pro911=
XM_005245000.3:c.2732C= XP_005245057.1:p.Pro911=
XM_005245001.1:c.2732C= XP_005245058.1:p.Pro911=
XM_005245005.1:c.2573C= XP_005245062.1:p.Pro858=
XM_005245006.3:c.2573C= XP_005245063.1:p.Pro858=
XM_011509330.1:c.2624C= XP_011507632.1:p.Pro875=
XM_011509331.1:c.2375C= XP_011507633.1:p.Pro792=
XM_005244999.3:c.2732C= XP_005245056.1:p.Pro911=
XM_005245000.4:c.2732C= XP_005245057.1:p.Pro911=
XM_005245001.2:c.2732C= XP_005245058.1:p.Pro911=
XM_005245005.2:c.2573C= XP_005245062.1:p.Pro858=
XM_005245006.5:c.2573C= XP_005245063.1:p.Pro858=
XM_017000744.1:c.2753C= XP_016856233.1:p.Pro918=
XM_017000745.2:c.2705C= XP_016856234.1:p.Pro902=
XM_017000746.1:c.2705C= XP_016856235.1:p.Pro902=
XM_017000748.1:c.2573C= XP_016856237.1:p.Pro858=
XM_017000749.1:c.2573C= XP_016856238.1:p.Pro858=
XM_024454305.1:c.2606C= XP_024310073.1:p.Pro869=
XM_024454306.1:c.1532C= XP_024310074.1:p.Pro511=
XR_002959801.1:n.2587C=
NM_015100.4:c.2732C= MANE Select NP_055915.2:p.Pro911=
NM_001194937.2:c.2705C= NP_001181866.1:p.Pro902=
NM_001194938.2:c.2546C= NP_001181867.1:p.Pro849=
NM_145796.4:c.2447C= NP_665739.3:p.Pro816=