Canonical Allele Identifier: CA341948688

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378706C>A (hg19) ; chr1:g.151406230C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406230C>A , CM000663.2:g.151406230C>A	GRCh38
NC_000001.10:g.151378706C>A , CM000663.1:g.151378706C>A	GRCh37
NC_000001.9:g.149645330C>A	NCBI36
NG_046601.1:g.58236G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2853G>T	ENSP00000518163.1:p.Glu951Asp
ENST00000392723.6:c.2646G>T	ENSP00000376484.1:p.Glu882Asp
ENST00000439756.2:c.2805G>T	ENSP00000390156.2:p.Glu935Asp
ENST00000703168.1:c.2826G>T	ENSP00000515214.1:p.Glu942Asp
ENST00000271715.7:c.2805G>T MANE Select	ENSP00000271715.2:p.Glu935Asp
ENST00000271715.6:c.2805G>T	ENSP00000271715.2:p.Glu935Asp
ENST00000358476.7:n.2953G>T
ENST00000368863.6:c.2520G>T	ENSP00000357856.2:p.Glu840Asp
ENST00000392723.5:c.2646G>T	ENSP00000376484.1:p.Glu882Asp
ENST00000409503.5:c.2778G>T	ENSP00000386836.1:p.Glu926Asp
ENST00000491586.5:c.2673G>T	ENSP00000418408.1:p.Glu891Asp
ENST00000531094.5:c.2619G>T	ENSP00000431259.1:p.Glu873Asp
NM_001194937.1:c.2778G>T	NP_001181866.1:p.Glu926Asp
NM_001194938.1:c.2619G>T	NP_001181867.1:p.Glu873Asp
NM_015100.3:c.2805G>T	NP_055915.2:p.Glu935Asp
NM_145796.3:c.2520G>T	NP_665739.3:p.Glu840Asp
NM_207171.2:c.2646G>T	NP_997054.1:p.Glu882Asp
XM_005244999.1:c.2805G>T	XP_005245056.1:p.Glu935Asp
XM_005245000.3:c.2805G>T	XP_005245057.1:p.Glu935Asp
XM_005245001.1:c.2805G>T	XP_005245058.1:p.Glu935Asp
XM_005245005.1:c.2646G>T	XP_005245062.1:p.Glu882Asp
XM_005245006.3:c.2646G>T	XP_005245063.1:p.Glu882Asp
XM_011509330.1:c.2697G>T	XP_011507632.1:p.Glu899Asp
XM_011509331.1:c.2448G>T	XP_011507633.1:p.Glu816Asp
XM_005244999.3:c.2805G>T	XP_005245056.1:p.Glu935Asp
XM_005245000.4:c.2805G>T	XP_005245057.1:p.Glu935Asp
XM_005245001.2:c.2805G>T	XP_005245058.1:p.Glu935Asp
XM_005245005.2:c.2646G>T	XP_005245062.1:p.Glu882Asp
XM_005245006.5:c.2646G>T	XP_005245063.1:p.Glu882Asp
XM_017000744.1:c.2826G>T	XP_016856233.1:p.Glu942Asp
XM_017000745.2:c.2778G>T	XP_016856234.1:p.Glu926Asp
XM_017000746.1:c.2778G>T	XP_016856235.1:p.Glu926Asp
XM_017000748.1:c.2646G>T	XP_016856237.1:p.Glu882Asp
XM_017000749.1:c.2646G>T	XP_016856238.1:p.Glu882Asp
XM_024454305.1:c.2679G>T	XP_024310073.1:p.Glu893Asp
XM_024454306.1:c.1605G>T	XP_024310074.1:p.Glu535Asp
XR_002959801.1:n.2660G>T
NM_015100.4:c.2805G>T MANE Select	NP_055915.2:p.Glu935Asp
NM_001194937.2:c.2778G>T	NP_001181866.1:p.Glu926Asp
NM_001194938.2:c.2619G>T	NP_001181867.1:p.Glu873Asp
NM_145796.4:c.2520G>T	NP_665739.3:p.Glu840Asp