Canonical Allele Identifier: CA2479570504

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406069G= , CM000663.2:g.151406069G=	GRCh38
NC_000001.10:g.151378545G= , CM000663.1:g.151378545G=	GRCh37
NC_000001.9:g.149645169G=	NCBI36
NG_046601.1:g.58397C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.3014C=	ENSP00000518163.1:p.Thr1005=
ENST00000392723.6:c.2807C=	ENSP00000376484.1:p.Thr936=
ENST00000439756.2:c.2966C=	ENSP00000390156.2:p.Thr989=
ENST00000703168.1:c.2987C=	ENSP00000515214.1:p.Thr996=
ENST00000271715.7:c.2966C= MANE Select	ENSP00000271715.2:p.Thr989=
ENST00000271715.6:c.2966C=	ENSP00000271715.2:p.Thr989=
ENST00000358476.7:n.3114C=
ENST00000368863.6:c.2681C=	ENSP00000357856.2:p.Thr894=
ENST00000392723.5:c.2807C=	ENSP00000376484.1:p.Thr936=
ENST00000409503.5:c.2939C=	ENSP00000386836.1:p.Thr980=
ENST00000491586.5:c.2834C=	ENSP00000418408.1:p.Thr945=
ENST00000531094.5:c.2780C=	ENSP00000431259.1:p.Thr927=
NM_001194937.1:c.2939C=	NP_001181866.1:p.Thr980=
NM_001194938.1:c.2780C=	NP_001181867.1:p.Thr927=
NM_015100.3:c.2966C=	NP_055915.2:p.Thr989=
NM_145796.3:c.2681C=	NP_665739.3:p.Thr894=
NM_207171.2:c.2807C=	NP_997054.1:p.Thr936=
XM_005244999.1:c.2966C=	XP_005245056.1:p.Thr989=
XM_005245000.3:c.2966C=	XP_005245057.1:p.Thr989=
XM_005245001.1:c.2966C=	XP_005245058.1:p.Thr989=
XM_005245005.1:c.2807C=	XP_005245062.1:p.Thr936=
XM_005245006.3:c.2807C=	XP_005245063.1:p.Thr936=
XM_011509330.1:c.2858C=	XP_011507632.1:p.Thr953=
XM_011509331.1:c.2609C=	XP_011507633.1:p.Thr870=
XM_005244999.3:c.2966C=	XP_005245056.1:p.Thr989=
XM_005245000.4:c.2966C=	XP_005245057.1:p.Thr989=
XM_005245001.2:c.2966C=	XP_005245058.1:p.Thr989=
XM_005245005.2:c.2807C=	XP_005245062.1:p.Thr936=
XM_005245006.5:c.2807C=	XP_005245063.1:p.Thr936=
XM_017000744.1:c.2987C=	XP_016856233.1:p.Thr996=
XM_017000745.2:c.2939C=	XP_016856234.1:p.Thr980=
XM_017000746.1:c.2939C=	XP_016856235.1:p.Thr980=
XM_017000748.1:c.2807C=	XP_016856237.1:p.Thr936=
XM_017000749.1:c.2807C=	XP_016856238.1:p.Thr936=
XM_024454305.1:c.2840C=	XP_024310073.1:p.Thr947=
XM_024454306.1:c.1766C=	XP_024310074.1:p.Thr589=
XR_002959801.1:n.2821C=
NM_015100.4:c.2966C= MANE Select	NP_055915.2:p.Thr989=
NM_001194937.2:c.2939C=	NP_001181866.1:p.Thr980=
NM_001194938.2:c.2780C=	NP_001181867.1:p.Thr927=
NM_145796.4:c.2681C=	NP_665739.3:p.Thr894=