Canonical Allele Identifier: CA526660648

Gene: POGZ

Linked Data

• dbSNP Id: rs1156412195
• gnomAD v2: 1-151378965-AGAG-A
• gnomAD v3: 1-151406489-AGAG-A
• gnomAD v4: 1-151406489-AGAG-A
• MyVariant Identifiers: chr1:g.151378966_151378968del (hg19) ; chr1:g.151406490_151406492del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406493_151406495del , CM000663.2:g.151406493_151406495del	GRCh38
NC_000001.10:g.151378969_151378971del , CM000663.1:g.151378969_151378971del	GRCh37
NC_000001.9:g.149645593_149645595del	NCBI36
NG_046601.1:g.57974_57976del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2619-28_2619-26del	ENSP00000518163.1:n.2619-28_2619-26del
ENST00000392723.6:c.2412-28_2412-26del	ENSP00000376484.1:n.2412-28_2412-26del
ENST00000439756.2:c.2571-28_2571-26del	ENSP00000390156.2:n.2571-28_2571-26del
ENST00000703168.1:c.2592-28_2592-26del	ENSP00000515214.1:n.2592-28_2592-26del
ENST00000271715.7:c.2571-28_2571-26del MANE Select	ENSP00000271715.2:n.2571-28_2571-26del
ENST00000271715.6:c.2571-28_2571-26del	ENSP00000271715.2:n.2571-28_2571-26del
ENST00000358476.7:n.2719-28_2719-26del
ENST00000368863.6:c.2286-28_2286-26del	ENSP00000357856.2:n.2286-28_2286-26del
ENST00000392723.5:c.2412-28_2412-26del	ENSP00000376484.1:n.2412-28_2412-26del
ENST00000409503.5:c.2544-28_2544-26del	ENSP00000386836.1:n.2544-28_2544-26del
ENST00000491586.5:c.2439-28_2439-26del	ENSP00000418408.1:n.2439-28_2439-26del
ENST00000529669.1:c.771-28_771-26del	ENSP00000432295.1:n.771-28_771-26del
ENST00000531094.5:c.2385-28_2385-26del	ENSP00000431259.1:n.2385-28_2385-26del
NM_001194937.1:c.2544-28_2544-26del	NP_001181866.1:n.2544-28_2544-26del
NM_001194938.1:c.2385-28_2385-26del	NP_001181867.1:n.2385-28_2385-26del
NM_015100.3:c.2571-28_2571-26del	NP_055915.2:n.2571-28_2571-26del
NM_145796.3:c.2286-28_2286-26del	NP_665739.3:n.2286-28_2286-26del
NM_207171.2:c.2412-28_2412-26del	NP_997054.1:n.2412-28_2412-26del
XM_005244999.1:c.2571-28_2571-26del	XP_005245056.1:n.2571-28_2571-26del
XM_005245000.3:c.2571-28_2571-26del	XP_005245057.1:n.2571-28_2571-26del
XM_005245001.1:c.2571-28_2571-26del	XP_005245058.1:n.2571-28_2571-26del
XM_005245005.1:c.2412-28_2412-26del	XP_005245062.1:n.2412-28_2412-26del
XM_005245006.3:c.2412-28_2412-26del	XP_005245063.1:n.2412-28_2412-26del
XM_011509330.1:c.2463-28_2463-26del	XP_011507632.1:n.2463-28_2463-26del
XM_011509331.1:c.2214-28_2214-26del	XP_011507633.1:n.2214-28_2214-26del
XR_921760.1:n.2399-28_2399-26del
XM_005244999.3:c.2571-28_2571-26del	XP_005245056.1:n.2571-28_2571-26del
XM_005245000.4:c.2571-28_2571-26del	XP_005245057.1:n.2571-28_2571-26del
XM_005245001.2:c.2571-28_2571-26del	XP_005245058.1:n.2571-28_2571-26del
XM_005245005.2:c.2412-28_2412-26del	XP_005245062.1:n.2412-28_2412-26del
XM_005245006.5:c.2412-28_2412-26del	XP_005245063.1:n.2412-28_2412-26del
XM_017000744.1:c.2592-28_2592-26del	XP_016856233.1:n.2592-28_2592-26del
XM_017000745.2:c.2544-28_2544-26del	XP_016856234.1:n.2544-28_2544-26del
XM_017000746.1:c.2544-28_2544-26del	XP_016856235.1:n.2544-28_2544-26del
XM_017000748.1:c.2412-28_2412-26del	XP_016856237.1:n.2412-28_2412-26del
XM_017000749.1:c.2412-28_2412-26del	XP_016856238.1:n.2412-28_2412-26del
XM_024454305.1:c.2445-28_2445-26del	XP_024310073.1:n.2445-28_2445-26del
XM_024454306.1:c.1371-28_1371-26del	XP_024310074.1:n.1371-28_1371-26del
XR_002959801.1:n.2426-28_2426-26del
NM_015100.4:c.2571-28_2571-26del MANE Select	NP_055915.2:n.2571-28_2571-26del
NM_001194937.2:c.2544-28_2544-26del	NP_001181866.1:n.2544-28_2544-26del
NM_001194938.2:c.2385-28_2385-26del	NP_001181867.1:n.2385-28_2385-26del
NM_145796.4:c.2286-28_2286-26del	NP_665739.3:n.2286-28_2286-26del