Canonical Allele Identifier: CA2479570716

Gene: POGZ

Linked Data

• dbSNP Id: rs1653669476
• gnomAD v4: 1-151406524-CAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406529_151406531del , CM000663.2:g.151406529_151406531del	GRCh38
NC_000001.10:g.151379005_151379007del , CM000663.1:g.151379005_151379007del	GRCh37
NC_000001.9:g.149645629_149645631del	NCBI36
NG_046601.1:g.57939_57941del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2619-63_2619-61del	ENSP00000518163.1:n.2619-63_2619-61del
ENST00000392723.6:c.2412-63_2412-61del	ENSP00000376484.1:n.2412-63_2412-61del
ENST00000439756.2:c.2571-63_2571-61del	ENSP00000390156.2:n.2571-63_2571-61del
ENST00000703168.1:c.2592-63_2592-61del	ENSP00000515214.1:n.2592-63_2592-61del
ENST00000271715.7:c.2571-63_2571-61del MANE Select	ENSP00000271715.2:n.2571-63_2571-61del
ENST00000271715.6:c.2571-63_2571-61del	ENSP00000271715.2:n.2571-63_2571-61del
ENST00000358476.7:n.2719-63_2719-61del
ENST00000368863.6:c.2286-63_2286-61del	ENSP00000357856.2:n.2286-63_2286-61del
ENST00000392723.5:c.2412-63_2412-61del	ENSP00000376484.1:n.2412-63_2412-61del
ENST00000409503.5:c.2544-63_2544-61del	ENSP00000386836.1:n.2544-63_2544-61del
ENST00000491586.5:c.2439-63_2439-61del	ENSP00000418408.1:n.2439-63_2439-61del
ENST00000529669.1:c.771-63_771-61del	ENSP00000432295.1:n.771-63_771-61del
ENST00000531094.5:c.2385-63_2385-61del	ENSP00000431259.1:n.2385-63_2385-61del
NM_001194937.1:c.2544-63_2544-61del	NP_001181866.1:n.2544-63_2544-61del
NM_001194938.1:c.2385-63_2385-61del	NP_001181867.1:n.2385-63_2385-61del
NM_015100.3:c.2571-63_2571-61del	NP_055915.2:n.2571-63_2571-61del
NM_145796.3:c.2286-63_2286-61del	NP_665739.3:n.2286-63_2286-61del
NM_207171.2:c.2412-63_2412-61del	NP_997054.1:n.2412-63_2412-61del
XM_005244999.1:c.2571-63_2571-61del	XP_005245056.1:n.2571-63_2571-61del
XM_005245000.3:c.2571-63_2571-61del	XP_005245057.1:n.2571-63_2571-61del
XM_005245001.1:c.2571-63_2571-61del	XP_005245058.1:n.2571-63_2571-61del
XM_005245005.1:c.2412-63_2412-61del	XP_005245062.1:n.2412-63_2412-61del
XM_005245006.3:c.2412-63_2412-61del	XP_005245063.1:n.2412-63_2412-61del
XM_011509330.1:c.2463-63_2463-61del	XP_011507632.1:n.2463-63_2463-61del
XM_011509331.1:c.2214-63_2214-61del	XP_011507633.1:n.2214-63_2214-61del
XR_921760.1:n.2399-63_2399-61del
XM_005244999.3:c.2571-63_2571-61del	XP_005245056.1:n.2571-63_2571-61del
XM_005245000.4:c.2571-63_2571-61del	XP_005245057.1:n.2571-63_2571-61del
XM_005245001.2:c.2571-63_2571-61del	XP_005245058.1:n.2571-63_2571-61del
XM_005245005.2:c.2412-63_2412-61del	XP_005245062.1:n.2412-63_2412-61del
XM_005245006.5:c.2412-63_2412-61del	XP_005245063.1:n.2412-63_2412-61del
XM_017000744.1:c.2592-63_2592-61del	XP_016856233.1:n.2592-63_2592-61del
XM_017000745.2:c.2544-63_2544-61del	XP_016856234.1:n.2544-63_2544-61del
XM_017000746.1:c.2544-63_2544-61del	XP_016856235.1:n.2544-63_2544-61del
XM_017000748.1:c.2412-63_2412-61del	XP_016856237.1:n.2412-63_2412-61del
XM_017000749.1:c.2412-63_2412-61del	XP_016856238.1:n.2412-63_2412-61del
XM_024454305.1:c.2445-63_2445-61del	XP_024310073.1:n.2445-63_2445-61del
XM_024454306.1:c.1371-63_1371-61del	XP_024310074.1:n.1371-63_1371-61del
XR_002959801.1:n.2426-63_2426-61del
NM_015100.4:c.2571-63_2571-61del MANE Select	NP_055915.2:n.2571-63_2571-61del
NM_001194937.2:c.2544-63_2544-61del	NP_001181866.1:n.2544-63_2544-61del
NM_001194938.2:c.2385-63_2385-61del	NP_001181867.1:n.2385-63_2385-61del
NM_145796.4:c.2286-63_2286-61del	NP_665739.3:n.2286-63_2286-61del