Canonical Allele Identifier: CA2479570611

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406333A= , CM000663.2:g.151406333A=	GRCh38
NC_000001.10:g.151378809A= , CM000663.1:g.151378809A=	GRCh37
NC_000001.9:g.149645433A=	NCBI36
NG_046601.1:g.58133T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2750T=	ENSP00000518163.1:p.Leu917=
ENST00000392723.6:c.2543T=	ENSP00000376484.1:p.Leu848=
ENST00000439756.2:c.2702T=	ENSP00000390156.2:p.Leu901=
ENST00000703168.1:c.2723T=	ENSP00000515214.1:p.Leu908=
ENST00000271715.7:c.2702T= MANE Select	ENSP00000271715.2:p.Leu901=
ENST00000271715.6:c.2702T=	ENSP00000271715.2:p.Leu901=
ENST00000358476.7:n.2850T=
ENST00000368863.6:c.2417T=	ENSP00000357856.2:p.Leu806=
ENST00000392723.5:c.2543T=	ENSP00000376484.1:p.Leu848=
ENST00000409503.5:c.2675T=	ENSP00000386836.1:p.Leu892=
ENST00000491586.5:c.2570T=	ENSP00000418408.1:p.Leu857=
ENST00000529669.1:c.902T=	ENSP00000432295.1:p.Leu301=
ENST00000531094.5:c.2516T=	ENSP00000431259.1:p.Leu839=
NM_001194937.1:c.2675T=	NP_001181866.1:p.Leu892=
NM_001194938.1:c.2516T=	NP_001181867.1:p.Leu839=
NM_015100.3:c.2702T=	NP_055915.2:p.Leu901=
NM_145796.3:c.2417T=	NP_665739.3:p.Leu806=
NM_207171.2:c.2543T=	NP_997054.1:p.Leu848=
XM_005244999.1:c.2702T=	XP_005245056.1:p.Leu901=
XM_005245000.3:c.2702T=	XP_005245057.1:p.Leu901=
XM_005245001.1:c.2702T=	XP_005245058.1:p.Leu901=
XM_005245005.1:c.2543T=	XP_005245062.1:p.Leu848=
XM_005245006.3:c.2543T=	XP_005245063.1:p.Leu848=
XM_011509330.1:c.2594T=	XP_011507632.1:p.Leu865=
XM_011509331.1:c.2345T=	XP_011507633.1:p.Leu782=
XM_005244999.3:c.2702T=	XP_005245056.1:p.Leu901=
XM_005245000.4:c.2702T=	XP_005245057.1:p.Leu901=
XM_005245001.2:c.2702T=	XP_005245058.1:p.Leu901=
XM_005245005.2:c.2543T=	XP_005245062.1:p.Leu848=
XM_005245006.5:c.2543T=	XP_005245063.1:p.Leu848=
XM_017000744.1:c.2723T=	XP_016856233.1:p.Leu908=
XM_017000745.2:c.2675T=	XP_016856234.1:p.Leu892=
XM_017000746.1:c.2675T=	XP_016856235.1:p.Leu892=
XM_017000748.1:c.2543T=	XP_016856237.1:p.Leu848=
XM_017000749.1:c.2543T=	XP_016856238.1:p.Leu848=
XM_024454305.1:c.2576T=	XP_024310073.1:p.Leu859=
XM_024454306.1:c.1502T=	XP_024310074.1:p.Leu501=
XR_002959801.1:n.2557T=
NM_015100.4:c.2702T= MANE Select	NP_055915.2:p.Leu901=
NM_001194937.2:c.2675T=	NP_001181866.1:p.Leu892=
NM_001194938.2:c.2516T=	NP_001181867.1:p.Leu839=
NM_145796.4:c.2417T=	NP_665739.3:p.Leu806=