Canonical Allele Identifier: CA2479581126

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151430669C= , CM000663.2:g.151430669C=	GRCh38
NC_000001.10:g.151403145C= , CM000663.1:g.151403145C=	GRCh37
NC_000001.9:g.149669769C=	NCBI36
NG_046601.1:g.33797G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.504G=	ENSP00000518163.1:p.Thr168=
ENST00000392723.6:c.297G=	ENSP00000376484.1:p.Thr99=
ENST00000439756.2:c.456G=	ENSP00000390156.2:p.Thr152=
ENST00000703168.1:c.477G=	ENSP00000515214.1:p.Thr159=
ENST00000703169.1:c.456G=	ENSP00000515215.1:p.Thr152=
ENST00000271715.7:c.456G= MANE Select	ENSP00000271715.2:p.Thr152=
ENST00000271715.6:c.456G=	ENSP00000271715.2:p.Thr152=
ENST00000358476.7:n.325G=
ENST00000368863.6:c.284-2256G=	ENSP00000357856.2:n.284-2256G=
ENST00000392723.5:c.297G=	ENSP00000376484.1:p.Thr99=
ENST00000409503.5:c.456G=	ENSP00000386836.1:p.Thr152=
ENST00000467287.5:n.334G=
ENST00000485040.5:n.485G=
ENST00000491586.5:c.297G=	ENSP00000418408.1:p.Thr99=
ENST00000531094.5:c.297G=	ENSP00000431259.1:p.Thr99=
NM_001194937.1:c.456G=	NP_001181866.1:p.Thr152=
NM_001194938.1:c.297G=	NP_001181867.1:p.Thr99=
NM_015100.3:c.456G=	NP_055915.2:p.Thr152=
NM_145796.3:c.284-2256G=	NP_665739.3:n.284-2256G=
NM_207171.2:c.297G=	NP_997054.1:p.Thr99=
XM_005244999.1:c.456G=	XP_005245056.1:p.Thr152=
XM_005245000.3:c.456G=	XP_005245057.1:p.Thr152=
XM_005245001.1:c.456G=	XP_005245058.1:p.Thr152=
XM_005245005.1:c.297G=	XP_005245062.1:p.Thr99=
XM_005245006.3:c.297G=	XP_005245063.1:p.Thr99=
XM_011509330.1:c.348G=	XP_011507632.1:p.Thr116=
XM_011509331.1:c.99G=	XP_011507633.1:p.Thr33=
XR_921760.1:n.457G=
XM_005244999.3:c.456G=	XP_005245056.1:p.Thr152=
XM_005245000.4:c.456G=	XP_005245057.1:p.Thr152=
XM_005245001.2:c.456G=	XP_005245058.1:p.Thr152=
XM_005245005.2:c.297G=	XP_005245062.1:p.Thr99=
XM_005245006.5:c.297G=	XP_005245063.1:p.Thr99=
XM_017000744.1:c.477G=	XP_016856233.1:p.Thr159=
XM_017000745.2:c.456G=	XP_016856234.1:p.Thr152=
XM_017000746.1:c.456G=	XP_016856235.1:p.Thr152=
XM_017000748.1:c.297G=	XP_016856237.1:p.Thr99=
XM_017000749.1:c.297G=	XP_016856238.1:p.Thr99=
XM_024454305.1:c.477G=	XP_024310073.1:p.Thr159=
XM_024454306.1:c.-1827G=	XP_024310074.1:n.-1827G=
XR_002959801.1:n.484G=
NM_015100.4:c.456G= MANE Select	NP_055915.2:p.Thr152=
NM_001194937.2:c.456G=	NP_001181866.1:p.Thr152=
NM_001194938.2:c.297G=	NP_001181867.1:p.Thr99=
NM_145796.4:c.284-2256G=	NP_665739.3:n.284-2256G=