Canonical Allele Identifier: CA341948715
Gene: POGZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151406231T>G , CM000663.2:g.151406231T>G GRCh38
NC_000001.10:g.151378707T>G , CM000663.1:g.151378707T>G GRCh37
NC_000001.9:g.149645331T>G NCBI36
NG_046601.1:g.58235A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000710270.1:c.2852A>C ENSP00000518163.1:p.Glu951Ala
ENST00000392723.6:c.2645A>C ENSP00000376484.1:p.Glu882Ala
ENST00000439756.2:c.2804A>C ENSP00000390156.2:p.Glu935Ala
ENST00000703168.1:c.2825A>C ENSP00000515214.1:p.Glu942Ala
ENST00000271715.7:c.2804A>C MANE Select ENSP00000271715.2:p.Glu935Ala
ENST00000271715.6:c.2804A>C ENSP00000271715.2:p.Glu935Ala
ENST00000358476.7:n.2952A>C
ENST00000368863.6:c.2519A>C ENSP00000357856.2:p.Glu840Ala
ENST00000392723.5:c.2645A>C ENSP00000376484.1:p.Glu882Ala
ENST00000409503.5:c.2777A>C ENSP00000386836.1:p.Glu926Ala
ENST00000491586.5:c.2672A>C ENSP00000418408.1:p.Glu891Ala
ENST00000531094.5:c.2618A>C ENSP00000431259.1:p.Glu873Ala
NM_001194937.1:c.2777A>C NP_001181866.1:p.Glu926Ala
NM_001194938.1:c.2618A>C NP_001181867.1:p.Glu873Ala
NM_015100.3:c.2804A>C NP_055915.2:p.Glu935Ala
NM_145796.3:c.2519A>C NP_665739.3:p.Glu840Ala
NM_207171.2:c.2645A>C NP_997054.1:p.Glu882Ala
XM_005244999.1:c.2804A>C XP_005245056.1:p.Glu935Ala
XM_005245000.3:c.2804A>C XP_005245057.1:p.Glu935Ala
XM_005245001.1:c.2804A>C XP_005245058.1:p.Glu935Ala
XM_005245005.1:c.2645A>C XP_005245062.1:p.Glu882Ala
XM_005245006.3:c.2645A>C XP_005245063.1:p.Glu882Ala
XM_011509330.1:c.2696A>C XP_011507632.1:p.Glu899Ala
XM_011509331.1:c.2447A>C XP_011507633.1:p.Glu816Ala
XM_005244999.3:c.2804A>C XP_005245056.1:p.Glu935Ala
XM_005245000.4:c.2804A>C XP_005245057.1:p.Glu935Ala
XM_005245001.2:c.2804A>C XP_005245058.1:p.Glu935Ala
XM_005245005.2:c.2645A>C XP_005245062.1:p.Glu882Ala
XM_005245006.5:c.2645A>C XP_005245063.1:p.Glu882Ala
XM_017000744.1:c.2825A>C XP_016856233.1:p.Glu942Ala
XM_017000745.2:c.2777A>C XP_016856234.1:p.Glu926Ala
XM_017000746.1:c.2777A>C XP_016856235.1:p.Glu926Ala
XM_017000748.1:c.2645A>C XP_016856237.1:p.Glu882Ala
XM_017000749.1:c.2645A>C XP_016856238.1:p.Glu882Ala
XM_024454305.1:c.2678A>C XP_024310073.1:p.Glu893Ala
XM_024454306.1:c.1604A>C XP_024310074.1:p.Glu535Ala
XR_002959801.1:n.2659A>C
NM_015100.4:c.2804A>C MANE Select NP_055915.2:p.Glu935Ala
NM_001194937.2:c.2777A>C NP_001181866.1:p.Glu926Ala
NM_001194938.2:c.2618A>C NP_001181867.1:p.Glu873Ala
NM_145796.4:c.2519A>C NP_665739.3:p.Glu840Ala