Canonical Allele Identifier: CA2479570542

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406177T= , CM000663.2:g.151406177T=	GRCh38
NC_000001.10:g.151378653T= , CM000663.1:g.151378653T=	GRCh37
NC_000001.9:g.149645277T=	NCBI36
NG_046601.1:g.58289A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2906A=	ENSP00000518163.1:p.Gln969=
ENST00000392723.6:c.2699A=	ENSP00000376484.1:p.Gln900=
ENST00000439756.2:c.2858A=	ENSP00000390156.2:p.Gln953=
ENST00000703168.1:c.2879A=	ENSP00000515214.1:p.Gln960=
ENST00000271715.7:c.2858A= MANE Select	ENSP00000271715.2:p.Gln953=
ENST00000271715.6:c.2858A=	ENSP00000271715.2:p.Gln953=
ENST00000358476.7:n.3006A=
ENST00000368863.6:c.2573A=	ENSP00000357856.2:p.Gln858=
ENST00000392723.5:c.2699A=	ENSP00000376484.1:p.Gln900=
ENST00000409503.5:c.2831A=	ENSP00000386836.1:p.Gln944=
ENST00000491586.5:c.2726A=	ENSP00000418408.1:p.Gln909=
ENST00000531094.5:c.2672A=	ENSP00000431259.1:p.Gln891=
NM_001194937.1:c.2831A=	NP_001181866.1:p.Gln944=
NM_001194938.1:c.2672A=	NP_001181867.1:p.Gln891=
NM_015100.3:c.2858A=	NP_055915.2:p.Gln953=
NM_145796.3:c.2573A=	NP_665739.3:p.Gln858=
NM_207171.2:c.2699A=	NP_997054.1:p.Gln900=
XM_005244999.1:c.2858A=	XP_005245056.1:p.Gln953=
XM_005245000.3:c.2858A=	XP_005245057.1:p.Gln953=
XM_005245001.1:c.2858A=	XP_005245058.1:p.Gln953=
XM_005245005.1:c.2699A=	XP_005245062.1:p.Gln900=
XM_005245006.3:c.2699A=	XP_005245063.1:p.Gln900=
XM_011509330.1:c.2750A=	XP_011507632.1:p.Gln917=
XM_011509331.1:c.2501A=	XP_011507633.1:p.Gln834=
XM_005244999.3:c.2858A=	XP_005245056.1:p.Gln953=
XM_005245000.4:c.2858A=	XP_005245057.1:p.Gln953=
XM_005245001.2:c.2858A=	XP_005245058.1:p.Gln953=
XM_005245005.2:c.2699A=	XP_005245062.1:p.Gln900=
XM_005245006.5:c.2699A=	XP_005245063.1:p.Gln900=
XM_017000744.1:c.2879A=	XP_016856233.1:p.Gln960=
XM_017000745.2:c.2831A=	XP_016856234.1:p.Gln944=
XM_017000746.1:c.2831A=	XP_016856235.1:p.Gln944=
XM_017000748.1:c.2699A=	XP_016856237.1:p.Gln900=
XM_017000749.1:c.2699A=	XP_016856238.1:p.Gln900=
XM_024454305.1:c.2732A=	XP_024310073.1:p.Gln911=
XM_024454306.1:c.1658A=	XP_024310074.1:p.Gln553=
XR_002959801.1:n.2713A=
NM_015100.4:c.2858A= MANE Select	NP_055915.2:p.Gln953=
NM_001194937.2:c.2831A=	NP_001181866.1:p.Gln944=
NM_001194938.2:c.2672A=	NP_001181867.1:p.Gln891=
NM_145796.4:c.2573A=	NP_665739.3:p.Gln858=