Canonical Allele Identifier: CA341945183

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378351C>A (hg19) ; chr1:g.151405875C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151405875C>A , CM000663.2:g.151405875C>A	GRCh38
NC_000001.10:g.151378351C>A , CM000663.1:g.151378351C>A	GRCh37
NC_000001.9:g.149644975C>A	NCBI36
NG_046601.1:g.58591G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.3208G>T	ENSP00000518163.1:p.Ala1070Ser
ENST00000392723.6:c.3001G>T	ENSP00000376484.1:p.Ala1001Ser
ENST00000439756.2:c.3160G>T	ENSP00000390156.2:p.Ala1054Ser
ENST00000703168.1:c.3181G>T	ENSP00000515214.1:p.Ala1061Ser
ENST00000271715.7:c.3160G>T MANE Select	ENSP00000271715.2:p.Ala1054Ser
ENST00000271715.6:c.3160G>T	ENSP00000271715.2:p.Ala1054Ser
ENST00000358476.7:n.3308G>T
ENST00000368863.6:c.2875G>T	ENSP00000357856.2:p.Ala959Ser
ENST00000392723.5:c.3001G>T	ENSP00000376484.1:p.Ala1001Ser
ENST00000409503.5:c.3133G>T	ENSP00000386836.1:p.Ala1045Ser
ENST00000491586.5:c.3028G>T	ENSP00000418408.1:p.Ala1010Ser
ENST00000531094.5:c.2974G>T	ENSP00000431259.1:p.Ala992Ser
NM_001194937.1:c.3133G>T	NP_001181866.1:p.Ala1045Ser
NM_001194938.1:c.2974G>T	NP_001181867.1:p.Ala992Ser
NM_015100.3:c.3160G>T	NP_055915.2:p.Ala1054Ser
NM_145796.3:c.2875G>T	NP_665739.3:p.Ala959Ser
NM_207171.2:c.3001G>T	NP_997054.1:p.Ala1001Ser
XM_005244999.1:c.3160G>T	XP_005245056.1:p.Ala1054Ser
XM_005245000.3:c.3160G>T	XP_005245057.1:p.Ala1054Ser
XM_005245001.1:c.3160G>T	XP_005245058.1:p.Ala1054Ser
XM_005245005.1:c.3001G>T	XP_005245062.1:p.Ala1001Ser
XM_005245006.3:c.3001G>T	XP_005245063.1:p.Ala1001Ser
XM_011509330.1:c.3052G>T	XP_011507632.1:p.Ala1018Ser
XM_011509331.1:c.2803G>T	XP_011507633.1:p.Ala935Ser
XM_005244999.3:c.3160G>T	XP_005245056.1:p.Ala1054Ser
XM_005245000.4:c.3160G>T	XP_005245057.1:p.Ala1054Ser
XM_005245001.2:c.3160G>T	XP_005245058.1:p.Ala1054Ser
XM_005245005.2:c.3001G>T	XP_005245062.1:p.Ala1001Ser
XM_005245006.5:c.3001G>T	XP_005245063.1:p.Ala1001Ser
XM_017000744.1:c.3181G>T	XP_016856233.1:p.Ala1061Ser
XM_017000745.2:c.3133G>T	XP_016856234.1:p.Ala1045Ser
XM_017000746.1:c.3133G>T	XP_016856235.1:p.Ala1045Ser
XM_017000748.1:c.3001G>T	XP_016856237.1:p.Ala1001Ser
XM_017000749.1:c.3001G>T	XP_016856238.1:p.Ala1001Ser
XM_024454305.1:c.3034G>T	XP_024310073.1:p.Ala1012Ser
XM_024454306.1:c.1960G>T	XP_024310074.1:p.Ala654Ser
XR_002959801.1:n.3015G>T
NM_015100.4:c.3160G>T MANE Select	NP_055915.2:p.Ala1054Ser
NM_001194937.2:c.3133G>T	NP_001181866.1:p.Ala1045Ser
NM_001194938.2:c.2974G>T	NP_001181867.1:p.Ala992Ser
NM_145796.4:c.2875G>T	NP_665739.3:p.Ala959Ser