Canonical Allele Identifier: CA2479581119

Gene: POGZ

Linked Data

• dbSNP Id: rs1658535124
• gnomAD v4: 1-151430646-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151430648del , CM000663.2:g.151430648del	GRCh38
NC_000001.10:g.151403124del , CM000663.1:g.151403124del	GRCh37
NC_000001.9:g.149669748del	NCBI36
NG_046601.1:g.33819del

Transcript Alleles

HGVS	Amino-acid change
ENST00000710270.1:c.507+19del	ENSP00000518163.1:n.507+19del
ENST00000392723.6:c.300+19del	ENSP00000376484.1:n.300+19del
ENST00000439756.2:c.459+19del	ENSP00000390156.2:n.459+19del
ENST00000703168.1:c.480+19del	ENSP00000515214.1:n.480+19del
ENST00000703169.1:c.459+19del	ENSP00000515215.1:n.459+19del
ENST00000271715.7:c.459+19del MANE Select	ENSP00000271715.2:n.459+19del
ENST00000271715.6:c.459+19del	ENSP00000271715.2:n.459+19del
ENST00000358476.7:n.328+19del
ENST00000368863.6:c.284-2234del	ENSP00000357856.2:n.284-2234del
ENST00000392723.5:c.300+19del	ENSP00000376484.1:n.300+19del
ENST00000409503.5:c.459+19del	ENSP00000386836.1:n.459+19del
ENST00000467287.5:n.337+19del
ENST00000485040.5:n.488+19del
ENST00000491586.5:c.300+19del	ENSP00000418408.1:n.300+19del
ENST00000531094.5:c.300+19del	ENSP00000431259.1:n.300+19del
NM_001194937.1:c.459+19del	NP_001181866.1:n.459+19del
NM_001194938.1:c.300+19del	NP_001181867.1:n.300+19del
NM_015100.3:c.459+19del	NP_055915.2:n.459+19del
NM_145796.3:c.284-2234del	NP_665739.3:n.284-2234del
NM_207171.2:c.300+19del	NP_997054.1:n.300+19del
XM_005244999.1:c.459+19del	XP_005245056.1:n.459+19del
XM_005245000.3:c.459+19del	XP_005245057.1:n.459+19del
XM_005245001.1:c.459+19del	XP_005245058.1:n.459+19del
XM_005245005.1:c.300+19del	XP_005245062.1:n.300+19del
XM_005245006.3:c.300+19del	XP_005245063.1:n.300+19del
XM_011509330.1:c.351+19del	XP_011507632.1:n.351+19del
XM_011509331.1:c.102+19del	XP_011507633.1:n.102+19del
XR_921760.1:n.460+19del
XM_005244999.3:c.459+19del	XP_005245056.1:n.459+19del
XM_005245000.4:c.459+19del	XP_005245057.1:n.459+19del
XM_005245001.2:c.459+19del	XP_005245058.1:n.459+19del
XM_005245005.2:c.300+19del	XP_005245062.1:n.300+19del
XM_005245006.5:c.300+19del	XP_005245063.1:n.300+19del
XM_017000744.1:c.480+19del	XP_016856233.1:n.480+19del
XM_017000745.2:c.459+19del	XP_016856234.1:n.459+19del
XM_017000746.1:c.459+19del	XP_016856235.1:n.459+19del
XM_017000748.1:c.300+19del	XP_016856237.1:n.300+19del
XM_017000749.1:c.300+19del	XP_016856238.1:n.300+19del
XM_024454305.1:c.480+19del	XP_024310073.1:n.480+19del
XM_024454306.1:c.-1824+19del	XP_024310074.1:n.-1824+19del
XR_002959801.1:n.487+19del
NM_015100.4:c.459+19del MANE Select	NP_055915.2:n.459+19del
NM_001194937.2:c.459+19del	NP_001181866.1:n.459+19del
NM_001194938.2:c.300+19del	NP_001181867.1:n.300+19del
NM_145796.4:c.284-2234del	NP_665739.3:n.284-2234del