Canonical Allele Identifier: CA2574056025
Gene: POGZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.151406531_151406532del , CM000663.2:g.151406531_151406532del GRCh38
NC_000001.10:g.151379007_151379008del , CM000663.1:g.151379007_151379008del GRCh37
NC_000001.9:g.149645631_149645632del NCBI36
NG_046601.1:g.57936_57937del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710270.1:c.2619-66_2619-65del ENSP00000518163.1:n.2619-66_2619-65del
ENST00000392723.6:c.2412-66_2412-65del ENSP00000376484.1:n.2412-66_2412-65del
ENST00000439756.2:c.2571-66_2571-65del ENSP00000390156.2:n.2571-66_2571-65del
ENST00000703168.1:c.2592-66_2592-65del ENSP00000515214.1:n.2592-66_2592-65del
ENST00000271715.7:c.2571-66_2571-65del MANE Select ENSP00000271715.2:n.2571-66_2571-65del
ENST00000271715.6:c.2571-66_2571-65del ENSP00000271715.2:n.2571-66_2571-65del
ENST00000358476.7:n.2719-66_2719-65del
ENST00000368863.6:c.2286-66_2286-65del ENSP00000357856.2:n.2286-66_2286-65del
ENST00000392723.5:c.2412-66_2412-65del ENSP00000376484.1:n.2412-66_2412-65del
ENST00000409503.5:c.2544-66_2544-65del ENSP00000386836.1:n.2544-66_2544-65del
ENST00000491586.5:c.2439-66_2439-65del ENSP00000418408.1:n.2439-66_2439-65del
ENST00000529669.1:c.771-66_771-65del ENSP00000432295.1:n.771-66_771-65del
ENST00000531094.5:c.2385-66_2385-65del ENSP00000431259.1:n.2385-66_2385-65del
NM_001194937.1:c.2544-66_2544-65del NP_001181866.1:n.2544-66_2544-65del
NM_001194938.1:c.2385-66_2385-65del NP_001181867.1:n.2385-66_2385-65del
NM_015100.3:c.2571-66_2571-65del NP_055915.2:n.2571-66_2571-65del
NM_145796.3:c.2286-66_2286-65del NP_665739.3:n.2286-66_2286-65del
NM_207171.2:c.2412-66_2412-65del NP_997054.1:n.2412-66_2412-65del
XM_005244999.1:c.2571-66_2571-65del XP_005245056.1:n.2571-66_2571-65del
XM_005245000.3:c.2571-66_2571-65del XP_005245057.1:n.2571-66_2571-65del
XM_005245001.1:c.2571-66_2571-65del XP_005245058.1:n.2571-66_2571-65del
XM_005245005.1:c.2412-66_2412-65del XP_005245062.1:n.2412-66_2412-65del
XM_005245006.3:c.2412-66_2412-65del XP_005245063.1:n.2412-66_2412-65del
XM_011509330.1:c.2463-66_2463-65del XP_011507632.1:n.2463-66_2463-65del
XM_011509331.1:c.2214-66_2214-65del XP_011507633.1:n.2214-66_2214-65del
XR_921760.1:n.2399-66_2399-65del
XM_005244999.3:c.2571-66_2571-65del XP_005245056.1:n.2571-66_2571-65del
XM_005245000.4:c.2571-66_2571-65del XP_005245057.1:n.2571-66_2571-65del
XM_005245001.2:c.2571-66_2571-65del XP_005245058.1:n.2571-66_2571-65del
XM_005245005.2:c.2412-66_2412-65del XP_005245062.1:n.2412-66_2412-65del
XM_005245006.5:c.2412-66_2412-65del XP_005245063.1:n.2412-66_2412-65del
XM_017000744.1:c.2592-66_2592-65del XP_016856233.1:n.2592-66_2592-65del
XM_017000745.2:c.2544-66_2544-65del XP_016856234.1:n.2544-66_2544-65del
XM_017000746.1:c.2544-66_2544-65del XP_016856235.1:n.2544-66_2544-65del
XM_017000748.1:c.2412-66_2412-65del XP_016856237.1:n.2412-66_2412-65del
XM_017000749.1:c.2412-66_2412-65del XP_016856238.1:n.2412-66_2412-65del
XM_024454305.1:c.2445-66_2445-65del XP_024310073.1:n.2445-66_2445-65del
XM_024454306.1:c.1371-66_1371-65del XP_024310074.1:n.1371-66_1371-65del
XR_002959801.1:n.2426-66_2426-65del
NM_015100.4:c.2571-66_2571-65del MANE Select NP_055915.2:n.2571-66_2571-65del
NM_001194937.2:c.2544-66_2544-65del NP_001181866.1:n.2544-66_2544-65del
NM_001194938.2:c.2385-66_2385-65del NP_001181867.1:n.2385-66_2385-65del
NM_145796.4:c.2286-66_2286-65del NP_665739.3:n.2286-66_2286-65del