Canonical Allele Identifier: CA2647924059

Gene: POGZ

Linked Data

• gnomAD v4: 1-151430651-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151430654_151430655del , CM000663.2:g.151430654_151430655del	GRCh38
NC_000001.10:g.151403130_151403131del , CM000663.1:g.151403130_151403131del	GRCh37
NC_000001.9:g.149669754_149669755del	NCBI36
NG_046601.1:g.33813_33814del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710270.1:c.507+13_507+14del	ENSP00000518163.1:n.507+13_507+14del
ENST00000392723.6:c.300+13_300+14del	ENSP00000376484.1:n.300+13_300+14del
ENST00000439756.2:c.459+13_459+14del	ENSP00000390156.2:n.459+13_459+14del
ENST00000703168.1:c.480+13_480+14del	ENSP00000515214.1:n.480+13_480+14del
ENST00000703169.1:c.459+13_459+14del	ENSP00000515215.1:n.459+13_459+14del
ENST00000271715.7:c.459+13_459+14del MANE Select	ENSP00000271715.2:n.459+13_459+14del
ENST00000271715.6:c.459+13_459+14del	ENSP00000271715.2:n.459+13_459+14del
ENST00000358476.7:n.328+13_328+14del
ENST00000368863.6:c.284-2240_284-2239del	ENSP00000357856.2:n.284-2240_284-2239del
ENST00000392723.5:c.300+13_300+14del	ENSP00000376484.1:n.300+13_300+14del
ENST00000409503.5:c.459+13_459+14del	ENSP00000386836.1:n.459+13_459+14del
ENST00000467287.5:n.337+13_337+14del
ENST00000485040.5:n.488+13_488+14del
ENST00000491586.5:c.300+13_300+14del	ENSP00000418408.1:n.300+13_300+14del
ENST00000531094.5:c.300+13_300+14del	ENSP00000431259.1:n.300+13_300+14del
NM_001194937.1:c.459+13_459+14del	NP_001181866.1:n.459+13_459+14del
NM_001194938.1:c.300+13_300+14del	NP_001181867.1:n.300+13_300+14del
NM_015100.3:c.459+13_459+14del	NP_055915.2:n.459+13_459+14del
NM_145796.3:c.284-2240_284-2239del	NP_665739.3:n.284-2240_284-2239del
NM_207171.2:c.300+13_300+14del	NP_997054.1:n.300+13_300+14del
XM_005244999.1:c.459+13_459+14del	XP_005245056.1:n.459+13_459+14del
XM_005245000.3:c.459+13_459+14del	XP_005245057.1:n.459+13_459+14del
XM_005245001.1:c.459+13_459+14del	XP_005245058.1:n.459+13_459+14del
XM_005245005.1:c.300+13_300+14del	XP_005245062.1:n.300+13_300+14del
XM_005245006.3:c.300+13_300+14del	XP_005245063.1:n.300+13_300+14del
XM_011509330.1:c.351+13_351+14del	XP_011507632.1:n.351+13_351+14del
XM_011509331.1:c.102+13_102+14del	XP_011507633.1:n.102+13_102+14del
XR_921760.1:n.460+13_460+14del
XM_005244999.3:c.459+13_459+14del	XP_005245056.1:n.459+13_459+14del
XM_005245000.4:c.459+13_459+14del	XP_005245057.1:n.459+13_459+14del
XM_005245001.2:c.459+13_459+14del	XP_005245058.1:n.459+13_459+14del
XM_005245005.2:c.300+13_300+14del	XP_005245062.1:n.300+13_300+14del
XM_005245006.5:c.300+13_300+14del	XP_005245063.1:n.300+13_300+14del
XM_017000744.1:c.480+13_480+14del	XP_016856233.1:n.480+13_480+14del
XM_017000745.2:c.459+13_459+14del	XP_016856234.1:n.459+13_459+14del
XM_017000746.1:c.459+13_459+14del	XP_016856235.1:n.459+13_459+14del
XM_017000748.1:c.300+13_300+14del	XP_016856237.1:n.300+13_300+14del
XM_017000749.1:c.300+13_300+14del	XP_016856238.1:n.300+13_300+14del
XM_024454305.1:c.480+13_480+14del	XP_024310073.1:n.480+13_480+14del
XM_024454306.1:c.-1824+13_-1824+14del	XP_024310074.1:n.-1824+13_-1824+14del
XR_002959801.1:n.487+13_487+14del
NM_015100.4:c.459+13_459+14del MANE Select	NP_055915.2:n.459+13_459+14del
NM_001194937.2:c.459+13_459+14del	NP_001181866.1:n.459+13_459+14del
NM_001194938.2:c.300+13_300+14del	NP_001181867.1:n.300+13_300+14del
NM_145796.4:c.284-2240_284-2239del	NP_665739.3:n.284-2240_284-2239del