Canonical Allele Identifier: CA2479570638

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406387_151406389delinsTTG , CM000663.2:g.151406387_151406389delinsTTG	GRCh38
NC_000001.10:g.151378863_151378865delinsTTG , CM000663.1:g.151378863_151378865delinsTTG	GRCh37
NC_000001.9:g.149645487_149645489delinsTTG	NCBI36
NG_046601.1:g.58077_58079delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2694_2696delinsCAA	ENSP00000518163.1:p.Asn898=
ENST00000392723.6:c.2487_2489delinsCAA	ENSP00000376484.1:p.Asn829=
ENST00000439756.2:c.2646_2648delinsCAA	ENSP00000390156.2:p.Asn882=
ENST00000703168.1:c.2667_2669delinsCAA	ENSP00000515214.1:p.Asn889=
ENST00000271715.7:c.2646_2648delinsCAA MANE Select	ENSP00000271715.2:p.Asn882=
ENST00000271715.6:c.2646_2648delinsCAA	ENSP00000271715.2:p.Asn882=
ENST00000358476.7:n.2794_2796delinsCAA
ENST00000368863.6:c.2361_2363delinsCAA	ENSP00000357856.2:p.Asn787=
ENST00000392723.5:c.2487_2489delinsCAA	ENSP00000376484.1:p.Asn829=
ENST00000409503.5:c.2619_2621delinsCAA	ENSP00000386836.1:p.Asn873=
ENST00000491586.5:c.2514_2516delinsCAA	ENSP00000418408.1:p.Asn838=
ENST00000529669.1:c.846_848delinsCAA	ENSP00000432295.1:p.Asn282=
ENST00000531094.5:c.2460_2462delinsCAA	ENSP00000431259.1:p.Asn820=
NM_001194937.1:c.2619_2621delinsCAA	NP_001181866.1:p.Asn873=
NM_001194938.1:c.2460_2462delinsCAA	NP_001181867.1:p.Asn820=
NM_015100.3:c.2646_2648delinsCAA	NP_055915.2:p.Asn882=
NM_145796.3:c.2361_2363delinsCAA	NP_665739.3:p.Asn787=
NM_207171.2:c.2487_2489delinsCAA	NP_997054.1:p.Asn829=
XM_005244999.1:c.2646_2648delinsCAA	XP_005245056.1:p.Asn882=
XM_005245000.3:c.2646_2648delinsCAA	XP_005245057.1:p.Asn882=
XM_005245001.1:c.2646_2648delinsCAA	XP_005245058.1:p.Asn882=
XM_005245005.1:c.2487_2489delinsCAA	XP_005245062.1:p.Asn829=
XM_005245006.3:c.2487_2489delinsCAA	XP_005245063.1:p.Asn829=
XM_011509330.1:c.2538_2540delinsCAA	XP_011507632.1:p.Asn846=
XM_011509331.1:c.2289_2291delinsCAA	XP_011507633.1:p.Asn763=
XM_005244999.3:c.2646_2648delinsCAA	XP_005245056.1:p.Asn882=
XM_005245000.4:c.2646_2648delinsCAA	XP_005245057.1:p.Asn882=
XM_005245001.2:c.2646_2648delinsCAA	XP_005245058.1:p.Asn882=
XM_005245005.2:c.2487_2489delinsCAA	XP_005245062.1:p.Asn829=
XM_005245006.5:c.2487_2489delinsCAA	XP_005245063.1:p.Asn829=
XM_017000744.1:c.2667_2669delinsCAA	XP_016856233.1:p.Asn889=
XM_017000745.2:c.2619_2621delinsCAA	XP_016856234.1:p.Asn873=
XM_017000746.1:c.2619_2621delinsCAA	XP_016856235.1:p.Asn873=
XM_017000748.1:c.2487_2489delinsCAA	XP_016856237.1:p.Asn829=
XM_017000749.1:c.2487_2489delinsCAA	XP_016856238.1:p.Asn829=
XM_024454305.1:c.2520_2522delinsCAA	XP_024310073.1:p.Asn840=
XM_024454306.1:c.1446_1448delinsCAA	XP_024310074.1:p.Asn482=
XR_002959801.1:n.2501_2503delinsCAA
NM_015100.4:c.2646_2648delinsCAA MANE Select	NP_055915.2:p.Asn882=
NM_001194937.2:c.2619_2621delinsCAA	NP_001181866.1:p.Asn873=
NM_001194938.2:c.2460_2462delinsCAA	NP_001181867.1:p.Asn820=
NM_145796.4:c.2361_2363delinsCAA	NP_665739.3:p.Asn787=