Canonical Allele Identifier: CA341972702

Gene: POGZ

Linked Data

• gnomAD v4: 1-151424965-C-T
• MyVariant Identifiers: chr1:g.151397441C>T (hg19) ; chr1:g.151424965C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151424965C>T , CM000663.2:g.151424965C>T	GRCh38
NC_000001.10:g.151397441C>T , CM000663.1:g.151397441C>T	GRCh37
NC_000001.9:g.149664065C>T	NCBI36
NG_046601.1:g.39501G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.1223G>A	ENSP00000518163.1:p.Gly408Asp
ENST00000392723.6:c.1016G>A	ENSP00000376484.1:p.Gly339Asp
ENST00000439756.2:c.1175G>A	ENSP00000390156.2:p.Gly392Asp
ENST00000703168.1:c.1196G>A	ENSP00000515214.1:p.Gly399Asp
ENST00000703169.1:c.1148G>A	ENSP00000515215.1:p.Gly383Asp
ENST00000271715.7:c.1175G>A MANE Select	ENSP00000271715.2:p.Gly392Asp
ENST00000271715.6:c.1175G>A	ENSP00000271715.2:p.Gly392Asp
ENST00000358476.7:n.1044G>A
ENST00000368863.6:c.890G>A	ENSP00000357856.2:p.Gly297Asp
ENST00000392723.5:c.1016G>A	ENSP00000376484.1:p.Gly339Asp
ENST00000409503.5:c.1148G>A	ENSP00000386836.1:p.Gly383Asp
ENST00000441516.1:c.159-679G>A
ENST00000491586.5:c.1016G>A	ENSP00000418408.1:p.Gly339Asp
ENST00000495253.1:n.330G>A
ENST00000531094.5:c.989G>A	ENSP00000431259.1:p.Gly330Asp
NM_001194937.1:c.1148G>A	NP_001181866.1:p.Gly383Asp
NM_001194938.1:c.989G>A	NP_001181867.1:p.Gly330Asp
NM_015100.3:c.1175G>A	NP_055915.2:p.Gly392Asp
NM_145796.3:c.890G>A	NP_665739.3:p.Gly297Asp
NM_207171.2:c.1016G>A	NP_997054.1:p.Gly339Asp
XM_005244999.1:c.1175G>A	XP_005245056.1:p.Gly392Asp
XM_005245000.3:c.1175G>A	XP_005245057.1:p.Gly392Asp
XM_005245001.1:c.1175G>A	XP_005245058.1:p.Gly392Asp
XM_005245005.1:c.1016G>A	XP_005245062.1:p.Gly339Asp
XM_005245006.3:c.1016G>A	XP_005245063.1:p.Gly339Asp
XM_011509330.1:c.1067G>A	XP_011507632.1:p.Gly356Asp
XM_011509331.1:c.818G>A	XP_011507633.1:p.Gly273Asp
XR_921760.1:n.1176G>A
XM_005244999.3:c.1175G>A	XP_005245056.1:p.Gly392Asp
XM_005245000.4:c.1175G>A	XP_005245057.1:p.Gly392Asp
XM_005245001.2:c.1175G>A	XP_005245058.1:p.Gly392Asp
XM_005245005.2:c.1016G>A	XP_005245062.1:p.Gly339Asp
XM_005245006.5:c.1016G>A	XP_005245063.1:p.Gly339Asp
XM_017000744.1:c.1196G>A	XP_016856233.1:p.Gly399Asp
XM_017000745.2:c.1148G>A	XP_016856234.1:p.Gly383Asp
XM_017000746.1:c.1148G>A	XP_016856235.1:p.Gly383Asp
XM_017000748.1:c.1016G>A	XP_016856237.1:p.Gly339Asp
XM_017000749.1:c.1016G>A	XP_016856238.1:p.Gly339Asp
XM_024454305.1:c.1196G>A	XP_024310073.1:p.Gly399Asp
XM_024454306.1:c.-15-679G>A	XP_024310074.1:n.-15-679G>A
XR_002959801.1:n.1203G>A
NM_015100.4:c.1175G>A MANE Select	NP_055915.2:p.Gly392Asp
NM_001194937.2:c.1148G>A	NP_001181866.1:p.Gly383Asp
NM_001194938.2:c.989G>A	NP_001181867.1:p.Gly330Asp
NM_145796.4:c.890G>A	NP_665739.3:p.Gly297Asp