Canonical Allele Identifier: CA2573901845
Gene: POGZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151430662_151430663dup , CM000663.2:g.151430662_151430663dup GRCh38
NC_000001.10:g.151403138_151403139dup , CM000663.1:g.151403138_151403139dup GRCh37
NC_000001.9:g.149669762_149669763dup NCBI36
NG_046601.1:g.33804_33805dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000710270.1:c.507+4_507+5dup ENSP00000518163.1:n.507+4_507+5dup
ENST00000392723.6:c.300+4_300+5dup ENSP00000376484.1:n.300+4_300+5dup
ENST00000439756.2:c.459+4_459+5dup ENSP00000390156.2:n.459+4_459+5dup
ENST00000703168.1:c.480+4_480+5dup ENSP00000515214.1:n.480+4_480+5dup
ENST00000703169.1:c.459+4_459+5dup ENSP00000515215.1:n.459+4_459+5dup
ENST00000271715.7:c.459+4_459+5dup MANE Select ENSP00000271715.2:n.459+4_459+5dup
ENST00000271715.6:c.459+4_459+5dup ENSP00000271715.2:n.459+4_459+5dup
ENST00000358476.7:n.328+4_328+5dup
ENST00000368863.6:c.284-2249_284-2248dup ENSP00000357856.2:n.284-2249_284-2248dup
ENST00000392723.5:c.300+4_300+5dup ENSP00000376484.1:n.300+4_300+5dup
ENST00000409503.5:c.459+4_459+5dup ENSP00000386836.1:n.459+4_459+5dup
ENST00000467287.5:n.337+4_337+5dup
ENST00000485040.5:n.488+4_488+5dup
ENST00000491586.5:c.300+4_300+5dup ENSP00000418408.1:n.300+4_300+5dup
ENST00000531094.5:c.300+4_300+5dup ENSP00000431259.1:n.300+4_300+5dup
NM_001194937.1:c.459+4_459+5dup NP_001181866.1:n.459+4_459+5dup
NM_001194938.1:c.300+4_300+5dup NP_001181867.1:n.300+4_300+5dup
NM_015100.3:c.459+4_459+5dup NP_055915.2:n.459+4_459+5dup
NM_145796.3:c.284-2249_284-2248dup NP_665739.3:n.284-2249_284-2248dup
NM_207171.2:c.300+4_300+5dup NP_997054.1:n.300+4_300+5dup
XM_005244999.1:c.459+4_459+5dup XP_005245056.1:n.459+4_459+5dup
XM_005245000.3:c.459+4_459+5dup XP_005245057.1:n.459+4_459+5dup
XM_005245001.1:c.459+4_459+5dup XP_005245058.1:n.459+4_459+5dup
XM_005245005.1:c.300+4_300+5dup XP_005245062.1:n.300+4_300+5dup
XM_005245006.3:c.300+4_300+5dup XP_005245063.1:n.300+4_300+5dup
XM_011509330.1:c.351+4_351+5dup XP_011507632.1:n.351+4_351+5dup
XM_011509331.1:c.102+4_102+5dup XP_011507633.1:n.102+4_102+5dup
XR_921760.1:n.460+4_460+5dup
XM_005244999.3:c.459+4_459+5dup XP_005245056.1:n.459+4_459+5dup
XM_005245000.4:c.459+4_459+5dup XP_005245057.1:n.459+4_459+5dup
XM_005245001.2:c.459+4_459+5dup XP_005245058.1:n.459+4_459+5dup
XM_005245005.2:c.300+4_300+5dup XP_005245062.1:n.300+4_300+5dup
XM_005245006.5:c.300+4_300+5dup XP_005245063.1:n.300+4_300+5dup
XM_017000744.1:c.480+4_480+5dup XP_016856233.1:n.480+4_480+5dup
XM_017000745.2:c.459+4_459+5dup XP_016856234.1:n.459+4_459+5dup
XM_017000746.1:c.459+4_459+5dup XP_016856235.1:n.459+4_459+5dup
XM_017000748.1:c.300+4_300+5dup XP_016856237.1:n.300+4_300+5dup
XM_017000749.1:c.300+4_300+5dup XP_016856238.1:n.300+4_300+5dup
XM_024454305.1:c.480+4_480+5dup XP_024310073.1:n.480+4_480+5dup
XM_024454306.1:c.-1824+4_-1824+5dup XP_024310074.1:n.-1824+4_-1824+5dup
XR_002959801.1:n.487+4_487+5dup
NM_015100.4:c.459+4_459+5dup MANE Select NP_055915.2:n.459+4_459+5dup
NM_001194937.2:c.459+4_459+5dup NP_001181866.1:n.459+4_459+5dup
NM_001194938.2:c.300+4_300+5dup NP_001181867.1:n.300+4_300+5dup
NM_145796.4:c.284-2249_284-2248dup NP_665739.3:n.284-2249_284-2248dup