Canonical Allele Identifier: CA2647922386

Gene: POGZ

Linked Data

• gnomAD v4: 1-151424893-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151424895del , CM000663.2:g.151424895del	GRCh38
NC_000001.10:g.151397371del , CM000663.1:g.151397371del	GRCh37
NC_000001.9:g.149663995del	NCBI36
NG_046601.1:g.39572del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.1233+61del	ENSP00000518163.1:n.1233+61del
ENST00000392723.6:c.1026+61del	ENSP00000376484.1:n.1026+61del
ENST00000439756.2:c.1185+61del	ENSP00000390156.2:n.1185+61del
ENST00000703168.1:c.1206+61del	ENSP00000515214.1:n.1206+61del
ENST00000703169.1:c.1158+61del	ENSP00000515215.1:n.1158+61del
ENST00000271715.7:c.1185+61del MANE Select	ENSP00000271715.2:n.1185+61del
ENST00000271715.6:c.1185+61del	ENSP00000271715.2:n.1185+61del
ENST00000358476.7:n.1054+61del
ENST00000368863.6:c.900+61del	ENSP00000357856.2:n.900+61del
ENST00000392723.5:c.1026+61del	ENSP00000376484.1:n.1026+61del
ENST00000409503.5:c.1158+61del	ENSP00000386836.1:n.1158+61del
ENST00000441516.1:c.159-608del
ENST00000491586.5:c.1026+61del	ENSP00000418408.1:n.1026+61del
ENST00000495253.1:n.340+61del
ENST00000531094.5:c.999+61del	ENSP00000431259.1:n.999+61del
NM_001194937.1:c.1158+61del	NP_001181866.1:n.1158+61del
NM_001194938.1:c.999+61del	NP_001181867.1:n.999+61del
NM_015100.3:c.1185+61del	NP_055915.2:n.1185+61del
NM_145796.3:c.900+61del	NP_665739.3:n.900+61del
NM_207171.2:c.1026+61del	NP_997054.1:n.1026+61del
XM_005244999.1:c.1185+61del	XP_005245056.1:n.1185+61del
XM_005245000.3:c.1185+61del	XP_005245057.1:n.1185+61del
XM_005245001.1:c.1185+61del	XP_005245058.1:n.1185+61del
XM_005245005.1:c.1026+61del	XP_005245062.1:n.1026+61del
XM_005245006.3:c.1026+61del	XP_005245063.1:n.1026+61del
XM_011509330.1:c.1077+61del	XP_011507632.1:n.1077+61del
XM_011509331.1:c.828+61del	XP_011507633.1:n.828+61del
XR_921760.1:n.1186+61del
XM_005244999.3:c.1185+61del	XP_005245056.1:n.1185+61del
XM_005245000.4:c.1185+61del	XP_005245057.1:n.1185+61del
XM_005245001.2:c.1185+61del	XP_005245058.1:n.1185+61del
XM_005245005.2:c.1026+61del	XP_005245062.1:n.1026+61del
XM_005245006.5:c.1026+61del	XP_005245063.1:n.1026+61del
XM_017000744.1:c.1206+61del	XP_016856233.1:n.1206+61del
XM_017000745.2:c.1158+61del	XP_016856234.1:n.1158+61del
XM_017000746.1:c.1158+61del	XP_016856235.1:n.1158+61del
XM_017000748.1:c.1026+61del	XP_016856237.1:n.1026+61del
XM_017000749.1:c.1026+61del	XP_016856238.1:n.1026+61del
XM_024454305.1:c.1206+61del	XP_024310073.1:n.1206+61del
XM_024454306.1:c.-15-608del	XP_024310074.1:n.-15-608del
XR_002959801.1:n.1213+61del
NM_015100.4:c.1185+61del MANE Select	NP_055915.2:n.1185+61del
NM_001194937.2:c.1158+61del	NP_001181866.1:n.1158+61del
NM_001194938.2:c.999+61del	NP_001181867.1:n.999+61del
NM_145796.4:c.900+61del	NP_665739.3:n.900+61del