Canonical Allele Identifier: CA2479570545

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406181T= , CM000663.2:g.151406181T=	GRCh38
NC_000001.10:g.151378657T= , CM000663.1:g.151378657T=	GRCh37
NC_000001.9:g.149645281T=	NCBI36
NG_046601.1:g.58285A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2902A=	ENSP00000518163.1:p.Thr968=
ENST00000392723.6:c.2695A=	ENSP00000376484.1:p.Thr899=
ENST00000439756.2:c.2854A=	ENSP00000390156.2:p.Thr952=
ENST00000703168.1:c.2875A=	ENSP00000515214.1:p.Thr959=
ENST00000271715.7:c.2854A= MANE Select	ENSP00000271715.2:p.Thr952=
ENST00000271715.6:c.2854A=	ENSP00000271715.2:p.Thr952=
ENST00000358476.7:n.3002A=
ENST00000368863.6:c.2569A=	ENSP00000357856.2:p.Thr857=
ENST00000392723.5:c.2695A=	ENSP00000376484.1:p.Thr899=
ENST00000409503.5:c.2827A=	ENSP00000386836.1:p.Thr943=
ENST00000491586.5:c.2722A=	ENSP00000418408.1:p.Thr908=
ENST00000531094.5:c.2668A=	ENSP00000431259.1:p.Thr890=
NM_001194937.1:c.2827A=	NP_001181866.1:p.Thr943=
NM_001194938.1:c.2668A=	NP_001181867.1:p.Thr890=
NM_015100.3:c.2854A=	NP_055915.2:p.Thr952=
NM_145796.3:c.2569A=	NP_665739.3:p.Thr857=
NM_207171.2:c.2695A=	NP_997054.1:p.Thr899=
XM_005244999.1:c.2854A=	XP_005245056.1:p.Thr952=
XM_005245000.3:c.2854A=	XP_005245057.1:p.Thr952=
XM_005245001.1:c.2854A=	XP_005245058.1:p.Thr952=
XM_005245005.1:c.2695A=	XP_005245062.1:p.Thr899=
XM_005245006.3:c.2695A=	XP_005245063.1:p.Thr899=
XM_011509330.1:c.2746A=	XP_011507632.1:p.Thr916=
XM_011509331.1:c.2497A=	XP_011507633.1:p.Thr833=
XM_005244999.3:c.2854A=	XP_005245056.1:p.Thr952=
XM_005245000.4:c.2854A=	XP_005245057.1:p.Thr952=
XM_005245001.2:c.2854A=	XP_005245058.1:p.Thr952=
XM_005245005.2:c.2695A=	XP_005245062.1:p.Thr899=
XM_005245006.5:c.2695A=	XP_005245063.1:p.Thr899=
XM_017000744.1:c.2875A=	XP_016856233.1:p.Thr959=
XM_017000745.2:c.2827A=	XP_016856234.1:p.Thr943=
XM_017000746.1:c.2827A=	XP_016856235.1:p.Thr943=
XM_017000748.1:c.2695A=	XP_016856237.1:p.Thr899=
XM_017000749.1:c.2695A=	XP_016856238.1:p.Thr899=
XM_024454305.1:c.2728A=	XP_024310073.1:p.Thr910=
XM_024454306.1:c.1654A=	XP_024310074.1:p.Thr552=
XR_002959801.1:n.2709A=
NM_015100.4:c.2854A= MANE Select	NP_055915.2:p.Thr952=
NM_001194937.2:c.2827A=	NP_001181866.1:p.Thr943=
NM_001194938.2:c.2668A=	NP_001181867.1:p.Thr890=
NM_145796.4:c.2569A=	NP_665739.3:p.Thr857=