Canonical Allele Identifier: CA2647920381

Gene: POGZ

Linked Data

• gnomAD v4: 1-151406487-GAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406488_151406489del , CM000663.2:g.151406488_151406489del	GRCh38
NC_000001.10:g.151378964_151378965del , CM000663.1:g.151378964_151378965del	GRCh37
NC_000001.9:g.149645588_149645589del	NCBI36
NG_046601.1:g.57977_57978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2619-25_2619-24del	ENSP00000518163.1:n.2619-25_2619-24del
ENST00000392723.6:c.2412-25_2412-24del	ENSP00000376484.1:n.2412-25_2412-24del
ENST00000439756.2:c.2571-25_2571-24del	ENSP00000390156.2:n.2571-25_2571-24del
ENST00000703168.1:c.2592-25_2592-24del	ENSP00000515214.1:n.2592-25_2592-24del
ENST00000271715.7:c.2571-25_2571-24del MANE Select	ENSP00000271715.2:n.2571-25_2571-24del
ENST00000271715.6:c.2571-25_2571-24del	ENSP00000271715.2:n.2571-25_2571-24del
ENST00000358476.7:n.2719-25_2719-24del
ENST00000368863.6:c.2286-25_2286-24del	ENSP00000357856.2:n.2286-25_2286-24del
ENST00000392723.5:c.2412-25_2412-24del	ENSP00000376484.1:n.2412-25_2412-24del
ENST00000409503.5:c.2544-25_2544-24del	ENSP00000386836.1:n.2544-25_2544-24del
ENST00000491586.5:c.2439-25_2439-24del	ENSP00000418408.1:n.2439-25_2439-24del
ENST00000529669.1:c.771-25_771-24del	ENSP00000432295.1:n.771-25_771-24del
ENST00000531094.5:c.2385-25_2385-24del	ENSP00000431259.1:n.2385-25_2385-24del
NM_001194937.1:c.2544-25_2544-24del	NP_001181866.1:n.2544-25_2544-24del
NM_001194938.1:c.2385-25_2385-24del	NP_001181867.1:n.2385-25_2385-24del
NM_015100.3:c.2571-25_2571-24del	NP_055915.2:n.2571-25_2571-24del
NM_145796.3:c.2286-25_2286-24del	NP_665739.3:n.2286-25_2286-24del
NM_207171.2:c.2412-25_2412-24del	NP_997054.1:n.2412-25_2412-24del
XM_005244999.1:c.2571-25_2571-24del	XP_005245056.1:n.2571-25_2571-24del
XM_005245000.3:c.2571-25_2571-24del	XP_005245057.1:n.2571-25_2571-24del
XM_005245001.1:c.2571-25_2571-24del	XP_005245058.1:n.2571-25_2571-24del
XM_005245005.1:c.2412-25_2412-24del	XP_005245062.1:n.2412-25_2412-24del
XM_005245006.3:c.2412-25_2412-24del	XP_005245063.1:n.2412-25_2412-24del
XM_011509330.1:c.2463-25_2463-24del	XP_011507632.1:n.2463-25_2463-24del
XM_011509331.1:c.2214-25_2214-24del	XP_011507633.1:n.2214-25_2214-24del
XR_921760.1:n.2399-25_2399-24del
XM_005244999.3:c.2571-25_2571-24del	XP_005245056.1:n.2571-25_2571-24del
XM_005245000.4:c.2571-25_2571-24del	XP_005245057.1:n.2571-25_2571-24del
XM_005245001.2:c.2571-25_2571-24del	XP_005245058.1:n.2571-25_2571-24del
XM_005245005.2:c.2412-25_2412-24del	XP_005245062.1:n.2412-25_2412-24del
XM_005245006.5:c.2412-25_2412-24del	XP_005245063.1:n.2412-25_2412-24del
XM_017000744.1:c.2592-25_2592-24del	XP_016856233.1:n.2592-25_2592-24del
XM_017000745.2:c.2544-25_2544-24del	XP_016856234.1:n.2544-25_2544-24del
XM_017000746.1:c.2544-25_2544-24del	XP_016856235.1:n.2544-25_2544-24del
XM_017000748.1:c.2412-25_2412-24del	XP_016856237.1:n.2412-25_2412-24del
XM_017000749.1:c.2412-25_2412-24del	XP_016856238.1:n.2412-25_2412-24del
XM_024454305.1:c.2445-25_2445-24del	XP_024310073.1:n.2445-25_2445-24del
XM_024454306.1:c.1371-25_1371-24del	XP_024310074.1:n.1371-25_1371-24del
XR_002959801.1:n.2426-25_2426-24del
NM_015100.4:c.2571-25_2571-24del MANE Select	NP_055915.2:n.2571-25_2571-24del
NM_001194937.2:c.2544-25_2544-24del	NP_001181866.1:n.2544-25_2544-24del
NM_001194938.2:c.2385-25_2385-24del	NP_001181867.1:n.2385-25_2385-24del
NM_145796.4:c.2286-25_2286-24del	NP_665739.3:n.2286-25_2286-24del