Canonical Allele Identifier: CA2574056133

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151408333del , CM000663.2:g.151408333del	GRCh38
NC_000001.10:g.151380809del , CM000663.1:g.151380809del	GRCh37
NC_000001.9:g.149647433del	NCBI36
NG_046601.1:g.56134del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2282+77del	ENSP00000518163.1:n.2282+77del
ENST00000392723.6:c.2075+77del	ENSP00000376484.1:n.2075+77del
ENST00000439756.2:c.2234+77del	ENSP00000390156.2:n.2234+77del
ENST00000703168.1:c.2255+77del	ENSP00000515214.1:n.2255+77del
ENST00000271715.7:c.2234+77del MANE Select	ENSP00000271715.2:n.2234+77del
ENST00000271715.6:c.2234+77del	ENSP00000271715.2:n.2234+77del
ENST00000358476.7:n.2103+77del
ENST00000368863.6:c.1949+77del	ENSP00000357856.2:n.1949+77del
ENST00000392723.5:c.2075+77del	ENSP00000376484.1:n.2075+77del
ENST00000409503.5:c.2207+77del	ENSP00000386836.1:n.2207+77del
ENST00000491586.5:c.2102+77del	ENSP00000418408.1:n.2102+77del
ENST00000492528.1:n.222del
ENST00000529669.1:c.434+77del	ENSP00000432295.1:n.434+77del
ENST00000531094.5:c.2048+77del	ENSP00000431259.1:n.2048+77del
NM_001194937.1:c.2207+77del	NP_001181866.1:n.2207+77del
NM_001194938.1:c.2048+77del	NP_001181867.1:n.2048+77del
NM_015100.3:c.2234+77del	NP_055915.2:n.2234+77del
NM_145796.3:c.1949+77del	NP_665739.3:n.1949+77del
NM_207171.2:c.2075+77del	NP_997054.1:n.2075+77del
XM_005244999.1:c.2234+77del	XP_005245056.1:n.2234+77del
XM_005245000.3:c.2234+77del	XP_005245057.1:n.2234+77del
XM_005245001.1:c.2234+77del	XP_005245058.1:n.2234+77del
XM_005245005.1:c.2075+77del	XP_005245062.1:n.2075+77del
XM_005245006.3:c.2075+77del	XP_005245063.1:n.2075+77del
XM_011509330.1:c.2126+77del	XP_011507632.1:n.2126+77del
XM_011509331.1:c.1877+77del	XP_011507633.1:n.1877+77del
XR_921760.1:n.2063-92del
XM_005244999.3:c.2234+77del	XP_005245056.1:n.2234+77del
XM_005245000.4:c.2234+77del	XP_005245057.1:n.2234+77del
XM_005245001.2:c.2234+77del	XP_005245058.1:n.2234+77del
XM_005245005.2:c.2075+77del	XP_005245062.1:n.2075+77del
XM_005245006.5:c.2075+77del	XP_005245063.1:n.2075+77del
XM_017000744.1:c.2255+77del	XP_016856233.1:n.2255+77del
XM_017000745.2:c.2207+77del	XP_016856234.1:n.2207+77del
XM_017000746.1:c.2207+77del	XP_016856235.1:n.2207+77del
XM_017000748.1:c.2075+77del	XP_016856237.1:n.2075+77del
XM_017000749.1:c.2075+77del	XP_016856238.1:n.2075+77del
XM_024454305.1:c.2108+77del	XP_024310073.1:n.2108+77del
XM_024454306.1:c.1034+77del	XP_024310074.1:n.1034+77del
XR_002959801.1:n.2090-92del
NM_015100.4:c.2234+77del MANE Select	NP_055915.2:n.2234+77del
NM_001194937.2:c.2207+77del	NP_001181866.1:n.2207+77del
NM_001194938.2:c.2048+77del	NP_001181867.1:n.2048+77del
NM_145796.4:c.1949+77del	NP_665739.3:n.1949+77del