Canonical Allele Identifier: CA2647920375

Gene: POGZ

Linked Data

• gnomAD v4: 1-151406202-GATC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406207_151406209del , CM000663.2:g.151406207_151406209del	GRCh38
NC_000001.10:g.151378683_151378685del , CM000663.1:g.151378683_151378685del	GRCh37
NC_000001.9:g.149645307_149645309del	NCBI36
NG_046601.1:g.58261_58263del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2878_2880del	ENSP00000518163.1:p.Asp960del
ENST00000392723.6:c.2671_2673del	ENSP00000376484.1:p.Asp891del
ENST00000439756.2:c.2830_2832del	ENSP00000390156.2:p.Asp944del
ENST00000703168.1:c.2851_2853del	ENSP00000515214.1:p.Asp951del
ENST00000271715.7:c.2830_2832del MANE Select	ENSP00000271715.2:p.Asp944del
ENST00000271715.6:c.2830_2832del	ENSP00000271715.2:p.Asp944del
ENST00000358476.7:n.2978_2980del
ENST00000368863.6:c.2545_2547del	ENSP00000357856.2:p.Asp849del
ENST00000392723.5:c.2671_2673del	ENSP00000376484.1:p.Asp891del
ENST00000409503.5:c.2803_2805del	ENSP00000386836.1:p.Asp935del
ENST00000491586.5:c.2698_2700del	ENSP00000418408.1:p.Asp900del
ENST00000531094.5:c.2644_2646del	ENSP00000431259.1:p.Asp882del
NM_001194937.1:c.2803_2805del	NP_001181866.1:p.Asp935del
NM_001194938.1:c.2644_2646del	NP_001181867.1:p.Asp882del
NM_015100.3:c.2830_2832del	NP_055915.2:p.Asp944del
NM_145796.3:c.2545_2547del	NP_665739.3:p.Asp849del
NM_207171.2:c.2671_2673del	NP_997054.1:p.Asp891del
XM_005244999.1:c.2830_2832del	XP_005245056.1:p.Asp944del
XM_005245000.3:c.2830_2832del	XP_005245057.1:p.Asp944del
XM_005245001.1:c.2830_2832del	XP_005245058.1:p.Asp944del
XM_005245005.1:c.2671_2673del	XP_005245062.1:p.Asp891del
XM_005245006.3:c.2671_2673del	XP_005245063.1:p.Asp891del
XM_011509330.1:c.2722_2724del	XP_011507632.1:p.Asp908del
XM_011509331.1:c.2473_2475del	XP_011507633.1:p.Asp825del
XM_005244999.3:c.2830_2832del	XP_005245056.1:p.Asp944del
XM_005245000.4:c.2830_2832del	XP_005245057.1:p.Asp944del
XM_005245001.2:c.2830_2832del	XP_005245058.1:p.Asp944del
XM_005245005.2:c.2671_2673del	XP_005245062.1:p.Asp891del
XM_005245006.5:c.2671_2673del	XP_005245063.1:p.Asp891del
XM_017000744.1:c.2851_2853del	XP_016856233.1:p.Asp951del
XM_017000745.2:c.2803_2805del	XP_016856234.1:p.Asp935del
XM_017000746.1:c.2803_2805del	XP_016856235.1:p.Asp935del
XM_017000748.1:c.2671_2673del	XP_016856237.1:p.Asp891del
XM_017000749.1:c.2671_2673del	XP_016856238.1:p.Asp891del
XM_024454305.1:c.2704_2706del	XP_024310073.1:p.Asp902del
XM_024454306.1:c.1630_1632del	XP_024310074.1:p.Asp544del
XR_002959801.1:n.2685_2687del
NM_015100.4:c.2830_2832del MANE Select	NP_055915.2:p.Asp944del
NM_001194937.2:c.2803_2805del	NP_001181866.1:p.Asp935del
NM_001194938.2:c.2644_2646del	NP_001181867.1:p.Asp882del
NM_145796.4:c.2545_2547del	NP_665739.3:p.Asp849del