Canonical Allele Identifier: CA2479581161
Gene: POGZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151430815C= , CM000663.2:g.151430815C= GRCh38
NC_000001.10:g.151403291C= , CM000663.1:g.151403291C= GRCh37
NC_000001.9:g.149669915C= NCBI36
NG_046601.1:g.33651G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710270.1:c.358G= ENSP00000518163.1:p.Gly120=
ENST00000392723.6:c.151G= ENSP00000376484.1:p.Gly51=
ENST00000439756.2:c.310G= ENSP00000390156.2:p.Gly104=
ENST00000703168.1:c.331G= ENSP00000515214.1:p.Gly111=
ENST00000703169.1:c.310G= ENSP00000515215.1:p.Gly104=
ENST00000271715.7:c.310G= MANE Select ENSP00000271715.2:p.Gly104=
ENST00000271715.6:c.310G= ENSP00000271715.2:p.Gly104=
ENST00000358476.7:n.179G=
ENST00000368863.6:c.284-2402G= ENSP00000357856.2:n.284-2402G=
ENST00000392723.5:c.151G= ENSP00000376484.1:p.Gly51=
ENST00000409503.5:c.310G= ENSP00000386836.1:p.Gly104=
ENST00000450842.1:c.151G= ENSP00000395332.1:p.Gly51=
ENST00000467287.5:n.188G=
ENST00000485040.5:n.339G=
ENST00000491586.5:c.151G= ENSP00000418408.1:p.Gly51=
ENST00000531094.5:c.151G= ENSP00000431259.1:p.Gly51=
ENST00000533351.5:c.310G= ENSP00000433637.1:p.Gly104=
ENST00000533461.5:c.310G= ENSP00000433934.1:p.Gly104=
NM_001194937.1:c.310G= NP_001181866.1:p.Gly104=
NM_001194938.1:c.151G= NP_001181867.1:p.Gly51=
NM_015100.3:c.310G= NP_055915.2:p.Gly104=
NM_145796.3:c.284-2402G= NP_665739.3:n.284-2402G=
NM_207171.2:c.151G= NP_997054.1:p.Gly51=
XM_005244999.1:c.310G= XP_005245056.1:p.Gly104=
XM_005245000.3:c.310G= XP_005245057.1:p.Gly104=
XM_005245001.1:c.310G= XP_005245058.1:p.Gly104=
XM_005245005.1:c.151G= XP_005245062.1:p.Gly51=
XM_005245006.3:c.151G= XP_005245063.1:p.Gly51=
XM_011509330.1:c.202G= XP_011507632.1:p.Gly68=
XM_011509331.1:c.-48G= XP_011507633.1:n.-48G=
XR_921760.1:n.311G=
XM_005244999.3:c.310G= XP_005245056.1:p.Gly104=
XM_005245000.4:c.310G= XP_005245057.1:p.Gly104=
XM_005245001.2:c.310G= XP_005245058.1:p.Gly104=
XM_005245005.2:c.151G= XP_005245062.1:p.Gly51=
XM_005245006.5:c.151G= XP_005245063.1:p.Gly51=
XM_017000744.1:c.331G= XP_016856233.1:p.Gly111=
XM_017000745.2:c.310G= XP_016856234.1:p.Gly104=
XM_017000746.1:c.310G= XP_016856235.1:p.Gly104=
XM_017000748.1:c.151G= XP_016856237.1:p.Gly51=
XM_017000749.1:c.151G= XP_016856238.1:p.Gly51=
XM_024454305.1:c.331G= XP_024310073.1:p.Gly111=
XM_024454306.1:c.-1973G= XP_024310074.1:n.-1973G=
XR_002959801.1:n.338G=
NM_015100.4:c.310G= MANE Select NP_055915.2:p.Gly104=
NM_001194937.2:c.310G= NP_001181866.1:p.Gly104=
NM_001194938.2:c.151G= NP_001181867.1:p.Gly51=
NM_145796.4:c.284-2402G= NP_665739.3:n.284-2402G=