Canonical Allele Identifier: CA341948924

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378735C>T (hg19) ; chr1:g.151406259C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406259C>T , CM000663.2:g.151406259C>T	GRCh38
NC_000001.10:g.151378735C>T , CM000663.1:g.151378735C>T	GRCh37
NC_000001.9:g.149645359C>T	NCBI36
NG_046601.1:g.58207G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2824G>A	ENSP00000518163.1:p.Ala942Thr
ENST00000392723.6:c.2617G>A	ENSP00000376484.1:p.Ala873Thr
ENST00000439756.2:c.2776G>A	ENSP00000390156.2:p.Ala926Thr
ENST00000703168.1:c.2797G>A	ENSP00000515214.1:p.Ala933Thr
ENST00000271715.7:c.2776G>A MANE Select	ENSP00000271715.2:p.Ala926Thr
ENST00000271715.6:c.2776G>A	ENSP00000271715.2:p.Ala926Thr
ENST00000358476.7:n.2924G>A
ENST00000368863.6:c.2491G>A	ENSP00000357856.2:p.Ala831Thr
ENST00000392723.5:c.2617G>A	ENSP00000376484.1:p.Ala873Thr
ENST00000409503.5:c.2749G>A	ENSP00000386836.1:p.Ala917Thr
ENST00000491586.5:c.2644G>A	ENSP00000418408.1:p.Ala882Thr
ENST00000531094.5:c.2590G>A	ENSP00000431259.1:p.Ala864Thr
NM_001194937.1:c.2749G>A	NP_001181866.1:p.Ala917Thr
NM_001194938.1:c.2590G>A	NP_001181867.1:p.Ala864Thr
NM_015100.3:c.2776G>A	NP_055915.2:p.Ala926Thr
NM_145796.3:c.2491G>A	NP_665739.3:p.Ala831Thr
NM_207171.2:c.2617G>A	NP_997054.1:p.Ala873Thr
XM_005244999.1:c.2776G>A	XP_005245056.1:p.Ala926Thr
XM_005245000.3:c.2776G>A	XP_005245057.1:p.Ala926Thr
XM_005245001.1:c.2776G>A	XP_005245058.1:p.Ala926Thr
XM_005245005.1:c.2617G>A	XP_005245062.1:p.Ala873Thr
XM_005245006.3:c.2617G>A	XP_005245063.1:p.Ala873Thr
XM_011509330.1:c.2668G>A	XP_011507632.1:p.Ala890Thr
XM_011509331.1:c.2419G>A	XP_011507633.1:p.Ala807Thr
XM_005244999.3:c.2776G>A	XP_005245056.1:p.Ala926Thr
XM_005245000.4:c.2776G>A	XP_005245057.1:p.Ala926Thr
XM_005245001.2:c.2776G>A	XP_005245058.1:p.Ala926Thr
XM_005245005.2:c.2617G>A	XP_005245062.1:p.Ala873Thr
XM_005245006.5:c.2617G>A	XP_005245063.1:p.Ala873Thr
XM_017000744.1:c.2797G>A	XP_016856233.1:p.Ala933Thr
XM_017000745.2:c.2749G>A	XP_016856234.1:p.Ala917Thr
XM_017000746.1:c.2749G>A	XP_016856235.1:p.Ala917Thr
XM_017000748.1:c.2617G>A	XP_016856237.1:p.Ala873Thr
XM_017000749.1:c.2617G>A	XP_016856238.1:p.Ala873Thr
XM_024454305.1:c.2650G>A	XP_024310073.1:p.Ala884Thr
XM_024454306.1:c.1576G>A	XP_024310074.1:p.Ala526Thr
XR_002959801.1:n.2631G>A
NM_015100.4:c.2776G>A MANE Select	NP_055915.2:p.Ala926Thr
NM_001194937.2:c.2749G>A	NP_001181866.1:p.Ala917Thr
NM_001194938.2:c.2590G>A	NP_001181867.1:p.Ala864Thr
NM_145796.4:c.2491G>A	NP_665739.3:p.Ala831Thr