Canonical Allele Identifier: CA29569379

Gene: POGZ

Linked Data

• dbSNP Id: rs764743518
• gnomAD v4: 1-151406292-C-T
• MyVariant Identifiers: chr1:g.151378768C>T (hg19) ; chr1:g.151406292C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406292C>T , CM000663.2:g.151406292C>T	GRCh38
NC_000001.10:g.151378768C>T , CM000663.1:g.151378768C>T	GRCh37
NC_000001.9:g.149645392C>T	NCBI36
NG_046601.1:g.58174G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2791G>A	ENSP00000518163.1:p.Ala931Thr
ENST00000392723.6:c.2584G>A	ENSP00000376484.1:p.Ala862Thr
ENST00000439756.2:c.2743G>A	ENSP00000390156.2:p.Ala915Thr
ENST00000703168.1:c.2764G>A	ENSP00000515214.1:p.Ala922Thr
ENST00000271715.7:c.2743G>A MANE Select	ENSP00000271715.2:p.Ala915Thr
ENST00000271715.6:c.2743G>A	ENSP00000271715.2:p.Ala915Thr
ENST00000358476.7:n.2891G>A
ENST00000368863.6:c.2458G>A	ENSP00000357856.2:p.Ala820Thr
ENST00000392723.5:c.2584G>A	ENSP00000376484.1:p.Ala862Thr
ENST00000409503.5:c.2716G>A	ENSP00000386836.1:p.Ala906Thr
ENST00000491586.5:c.2611G>A	ENSP00000418408.1:p.Ala871Thr
ENST00000529669.1:c.943G>A	ENSP00000432295.1:p.Ala315Thr
ENST00000531094.5:c.2557G>A	ENSP00000431259.1:p.Ala853Thr
NM_001194937.1:c.2716G>A	NP_001181866.1:p.Ala906Thr
NM_001194938.1:c.2557G>A	NP_001181867.1:p.Ala853Thr
NM_015100.3:c.2743G>A	NP_055915.2:p.Ala915Thr
NM_145796.3:c.2458G>A	NP_665739.3:p.Ala820Thr
NM_207171.2:c.2584G>A	NP_997054.1:p.Ala862Thr
XM_005244999.1:c.2743G>A	XP_005245056.1:p.Ala915Thr
XM_005245000.3:c.2743G>A	XP_005245057.1:p.Ala915Thr
XM_005245001.1:c.2743G>A	XP_005245058.1:p.Ala915Thr
XM_005245005.1:c.2584G>A	XP_005245062.1:p.Ala862Thr
XM_005245006.3:c.2584G>A	XP_005245063.1:p.Ala862Thr
XM_011509330.1:c.2635G>A	XP_011507632.1:p.Ala879Thr
XM_011509331.1:c.2386G>A	XP_011507633.1:p.Ala796Thr
XM_005244999.3:c.2743G>A	XP_005245056.1:p.Ala915Thr
XM_005245000.4:c.2743G>A	XP_005245057.1:p.Ala915Thr
XM_005245001.2:c.2743G>A	XP_005245058.1:p.Ala915Thr
XM_005245005.2:c.2584G>A	XP_005245062.1:p.Ala862Thr
XM_005245006.5:c.2584G>A	XP_005245063.1:p.Ala862Thr
XM_017000744.1:c.2764G>A	XP_016856233.1:p.Ala922Thr
XM_017000745.2:c.2716G>A	XP_016856234.1:p.Ala906Thr
XM_017000746.1:c.2716G>A	XP_016856235.1:p.Ala906Thr
XM_017000748.1:c.2584G>A	XP_016856237.1:p.Ala862Thr
XM_017000749.1:c.2584G>A	XP_016856238.1:p.Ala862Thr
XM_024454305.1:c.2617G>A	XP_024310073.1:p.Ala873Thr
XM_024454306.1:c.1543G>A	XP_024310074.1:p.Ala515Thr
XR_002959801.1:n.2598G>A
NM_015100.4:c.2743G>A MANE Select	NP_055915.2:p.Ala915Thr
NM_001194937.2:c.2716G>A	NP_001181866.1:p.Ala906Thr
NM_001194938.2:c.2557G>A	NP_001181867.1:p.Ala853Thr
NM_145796.4:c.2458G>A	NP_665739.3:p.Ala820Thr