Canonical Allele Identifier: CA420909896

Gene: POGZ

Linked Data

• gnomAD v4: 1-151406431-C-A
• MyVariant Identifiers: chr1:g.151378907C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406431C>A , CM000663.2:g.151406431C>A	GRCh38
NC_000001.10:g.151378907C>A , CM000663.1:g.151378907C>A	GRCh37
NC_000001.9:g.149645531C>A	NCBI36
NG_046601.1:g.58035G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2652G>T	ENSP00000518163.1:p.Arg884=
ENST00000392723.6:c.2445G>T	ENSP00000376484.1:p.Arg815=
ENST00000439756.2:c.2604G>T	ENSP00000390156.2:p.Arg868=
ENST00000703168.1:c.2625G>T	ENSP00000515214.1:p.Arg875=
ENST00000271715.7:c.2604G>T MANE Select	ENSP00000271715.2:p.Arg868=
ENST00000271715.6:c.2604G>T	ENSP00000271715.2:p.Arg868=
ENST00000358476.7:n.2752G>T
ENST00000368863.6:c.2319G>T	ENSP00000357856.2:p.Arg773=
ENST00000392723.5:c.2445G>T	ENSP00000376484.1:p.Arg815=
ENST00000409503.5:c.2577G>T	ENSP00000386836.1:p.Arg859=
ENST00000491586.5:c.2472G>T	ENSP00000418408.1:p.Arg824=
ENST00000529669.1:c.804G>T	ENSP00000432295.1:p.Arg268=
ENST00000531094.5:c.2418G>T	ENSP00000431259.1:p.Arg806=
NM_001194937.1:c.2577G>T	NP_001181866.1:p.Arg859=
NM_001194938.1:c.2418G>T	NP_001181867.1:p.Arg806=
NM_015100.3:c.2604G>T	NP_055915.2:p.Arg868=
NM_145796.3:c.2319G>T	NP_665739.3:p.Arg773=
NM_207171.2:c.2445G>T	NP_997054.1:p.Arg815=
XM_005244999.1:c.2604G>T	XP_005245056.1:p.Arg868=
XM_005245000.3:c.2604G>T	XP_005245057.1:p.Arg868=
XM_005245001.1:c.2604G>T	XP_005245058.1:p.Arg868=
XM_005245005.1:c.2445G>T	XP_005245062.1:p.Arg815=
XM_005245006.3:c.2445G>T	XP_005245063.1:p.Arg815=
XM_011509330.1:c.2496G>T	XP_011507632.1:p.Arg832=
XM_011509331.1:c.2247G>T	XP_011507633.1:p.Arg749=
XR_921760.1:n.2432G>T
XM_005244999.3:c.2604G>T	XP_005245056.1:p.Arg868=
XM_005245000.4:c.2604G>T	XP_005245057.1:p.Arg868=
XM_005245001.2:c.2604G>T	XP_005245058.1:p.Arg868=
XM_005245005.2:c.2445G>T	XP_005245062.1:p.Arg815=
XM_005245006.5:c.2445G>T	XP_005245063.1:p.Arg815=
XM_017000744.1:c.2625G>T	XP_016856233.1:p.Arg875=
XM_017000745.2:c.2577G>T	XP_016856234.1:p.Arg859=
XM_017000746.1:c.2577G>T	XP_016856235.1:p.Arg859=
XM_017000748.1:c.2445G>T	XP_016856237.1:p.Arg815=
XM_017000749.1:c.2445G>T	XP_016856238.1:p.Arg815=
XM_024454305.1:c.2478G>T	XP_024310073.1:p.Arg826=
XM_024454306.1:c.1404G>T	XP_024310074.1:p.Arg468=
XR_002959801.1:n.2459G>T
NM_015100.4:c.2604G>T MANE Select	NP_055915.2:p.Arg868=
NM_001194937.2:c.2577G>T	NP_001181866.1:p.Arg859=
NM_001194938.2:c.2418G>T	NP_001181867.1:p.Arg806=
NM_145796.4:c.2319G>T	NP_665739.3:p.Arg773=