Canonical Allele Identifier: CA341949476

Gene: POGZ

Linked Data

• dbSNP Id: rs1653600411
• MyVariant Identifiers: chr1:g.151378818T>G (hg19) ; chr1:g.151406342T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406342T>G , CM000663.2:g.151406342T>G	GRCh38
NC_000001.10:g.151378818T>G , CM000663.1:g.151378818T>G	GRCh37
NC_000001.9:g.149645442T>G	NCBI36
NG_046601.1:g.58124A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2741A>C	ENSP00000518163.1:p.Glu914Ala
ENST00000392723.6:c.2534A>C	ENSP00000376484.1:p.Glu845Ala
ENST00000439756.2:c.2693A>C	ENSP00000390156.2:p.Glu898Ala
ENST00000703168.1:c.2714A>C	ENSP00000515214.1:p.Glu905Ala
ENST00000271715.7:c.2693A>C MANE Select	ENSP00000271715.2:p.Glu898Ala
ENST00000271715.6:c.2693A>C	ENSP00000271715.2:p.Glu898Ala
ENST00000358476.7:n.2841A>C
ENST00000368863.6:c.2408A>C	ENSP00000357856.2:p.Glu803Ala
ENST00000392723.5:c.2534A>C	ENSP00000376484.1:p.Glu845Ala
ENST00000409503.5:c.2666A>C	ENSP00000386836.1:p.Glu889Ala
ENST00000491586.5:c.2561A>C	ENSP00000418408.1:p.Glu854Ala
ENST00000529669.1:c.893A>C	ENSP00000432295.1:p.Glu298Ala
ENST00000531094.5:c.2507A>C	ENSP00000431259.1:p.Glu836Ala
NM_001194937.1:c.2666A>C	NP_001181866.1:p.Glu889Ala
NM_001194938.1:c.2507A>C	NP_001181867.1:p.Glu836Ala
NM_015100.3:c.2693A>C	NP_055915.2:p.Glu898Ala
NM_145796.3:c.2408A>C	NP_665739.3:p.Glu803Ala
NM_207171.2:c.2534A>C	NP_997054.1:p.Glu845Ala
XM_005244999.1:c.2693A>C	XP_005245056.1:p.Glu898Ala
XM_005245000.3:c.2693A>C	XP_005245057.1:p.Glu898Ala
XM_005245001.1:c.2693A>C	XP_005245058.1:p.Glu898Ala
XM_005245005.1:c.2534A>C	XP_005245062.1:p.Glu845Ala
XM_005245006.3:c.2534A>C	XP_005245063.1:p.Glu845Ala
XM_011509330.1:c.2585A>C	XP_011507632.1:p.Glu862Ala
XM_011509331.1:c.2336A>C	XP_011507633.1:p.Glu779Ala
XM_005244999.3:c.2693A>C	XP_005245056.1:p.Glu898Ala
XM_005245000.4:c.2693A>C	XP_005245057.1:p.Glu898Ala
XM_005245001.2:c.2693A>C	XP_005245058.1:p.Glu898Ala
XM_005245005.2:c.2534A>C	XP_005245062.1:p.Glu845Ala
XM_005245006.5:c.2534A>C	XP_005245063.1:p.Glu845Ala
XM_017000744.1:c.2714A>C	XP_016856233.1:p.Glu905Ala
XM_017000745.2:c.2666A>C	XP_016856234.1:p.Glu889Ala
XM_017000746.1:c.2666A>C	XP_016856235.1:p.Glu889Ala
XM_017000748.1:c.2534A>C	XP_016856237.1:p.Glu845Ala
XM_017000749.1:c.2534A>C	XP_016856238.1:p.Glu845Ala
XM_024454305.1:c.2567A>C	XP_024310073.1:p.Glu856Ala
XM_024454306.1:c.1493A>C	XP_024310074.1:p.Glu498Ala
XR_002959801.1:n.2548A>C
NM_015100.4:c.2693A>C MANE Select	NP_055915.2:p.Glu898Ala
NM_001194937.2:c.2666A>C	NP_001181866.1:p.Glu889Ala
NM_001194938.2:c.2507A>C	NP_001181867.1:p.Glu836Ala
NM_145796.4:c.2408A>C	NP_665739.3:p.Glu803Ala