Canonical Allele Identifier: CA2479570635

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406379_151406380delinsTG , CM000663.2:g.151406379_151406380delinsTG	GRCh38
NC_000001.10:g.151378855_151378856delinsTG , CM000663.1:g.151378855_151378856delinsTG	GRCh37
NC_000001.9:g.149645479_149645480delinsTG	NCBI36
NG_046601.1:g.58086_58087delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2703_2704delinsCA	ENSP00000518163.1:p.Ala901=
ENST00000392723.6:c.2496_2497delinsCA	ENSP00000376484.1:p.Ala832=
ENST00000439756.2:c.2655_2656delinsCA	ENSP00000390156.2:p.Ala885=
ENST00000703168.1:c.2676_2677delinsCA	ENSP00000515214.1:p.Ala892=
ENST00000271715.7:c.2655_2656delinsCA MANE Select	ENSP00000271715.2:p.Ala885=
ENST00000271715.6:c.2655_2656delinsCA	ENSP00000271715.2:p.Ala885=
ENST00000358476.7:n.2803_2804delinsCA
ENST00000368863.6:c.2370_2371delinsCA	ENSP00000357856.2:p.Ala790=
ENST00000392723.5:c.2496_2497delinsCA	ENSP00000376484.1:p.Ala832=
ENST00000409503.5:c.2628_2629delinsCA	ENSP00000386836.1:p.Ala876=
ENST00000491586.5:c.2523_2524delinsCA	ENSP00000418408.1:p.Ala841=
ENST00000529669.1:c.855_856delinsCA	ENSP00000432295.1:p.Ala285=
ENST00000531094.5:c.2469_2470delinsCA	ENSP00000431259.1:p.Ala823=
NM_001194937.1:c.2628_2629delinsCA	NP_001181866.1:p.Ala876=
NM_001194938.1:c.2469_2470delinsCA	NP_001181867.1:p.Ala823=
NM_015100.3:c.2655_2656delinsCA	NP_055915.2:p.Ala885=
NM_145796.3:c.2370_2371delinsCA	NP_665739.3:p.Ala790=
NM_207171.2:c.2496_2497delinsCA	NP_997054.1:p.Ala832=
XM_005244999.1:c.2655_2656delinsCA	XP_005245056.1:p.Ala885=
XM_005245000.3:c.2655_2656delinsCA	XP_005245057.1:p.Ala885=
XM_005245001.1:c.2655_2656delinsCA	XP_005245058.1:p.Ala885=
XM_005245005.1:c.2496_2497delinsCA	XP_005245062.1:p.Ala832=
XM_005245006.3:c.2496_2497delinsCA	XP_005245063.1:p.Ala832=
XM_011509330.1:c.2547_2548delinsCA	XP_011507632.1:p.Ala849=
XM_011509331.1:c.2298_2299delinsCA	XP_011507633.1:p.Ala766=
XM_005244999.3:c.2655_2656delinsCA	XP_005245056.1:p.Ala885=
XM_005245000.4:c.2655_2656delinsCA	XP_005245057.1:p.Ala885=
XM_005245001.2:c.2655_2656delinsCA	XP_005245058.1:p.Ala885=
XM_005245005.2:c.2496_2497delinsCA	XP_005245062.1:p.Ala832=
XM_005245006.5:c.2496_2497delinsCA	XP_005245063.1:p.Ala832=
XM_017000744.1:c.2676_2677delinsCA	XP_016856233.1:p.Ala892=
XM_017000745.2:c.2628_2629delinsCA	XP_016856234.1:p.Ala876=
XM_017000746.1:c.2628_2629delinsCA	XP_016856235.1:p.Ala876=
XM_017000748.1:c.2496_2497delinsCA	XP_016856237.1:p.Ala832=
XM_017000749.1:c.2496_2497delinsCA	XP_016856238.1:p.Ala832=
XM_024454305.1:c.2529_2530delinsCA	XP_024310073.1:p.Ala843=
XM_024454306.1:c.1455_1456delinsCA	XP_024310074.1:p.Ala485=
XR_002959801.1:n.2510_2511delinsCA
NM_015100.4:c.2655_2656delinsCA MANE Select	NP_055915.2:p.Ala885=
NM_001194937.2:c.2628_2629delinsCA	NP_001181866.1:p.Ala876=
NM_001194938.2:c.2469_2470delinsCA	NP_001181867.1:p.Ala823=
NM_145796.4:c.2370_2371delinsCA	NP_665739.3:p.Ala790=