Canonical Allele Identifier: CA916082084

Gene: POGZ

Linked Data

• ClinVar Variation Id: 842730
• ClinVar RCV Id: RCV001045197
• dbSNP Id: rs1653645674

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406459_151406466del , CM000663.2:g.151406459_151406466del	GRCh38
NC_000001.10:g.151378935_151378942del , CM000663.1:g.151378935_151378942del	GRCh37
NC_000001.9:g.149645559_149645566del	NCBI36
NG_046601.1:g.58000_58007del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2619-2_2624del
ENST00000392723.6:c.2412-2_2417del
ENST00000439756.2:c.2571-2_2576del
ENST00000703168.1:c.2592-2_2597del
ENST00000271715.7:c.2571-2_2576del
ENST00000271715.6:c.2571-2_2576del
ENST00000358476.7:n.2719-2_2724del
ENST00000368863.6:c.2286-2_2291del
ENST00000392723.5:c.2412-2_2417del
ENST00000409503.5:c.2544-2_2549del
ENST00000491586.5:c.2439-2_2444del
ENST00000529669.1:c.771-2_776del
ENST00000531094.5:c.2385-2_2390del
NM_001194937.1:c.2544-2_2549del
NM_001194938.1:c.2385-2_2390del
NM_015100.3:c.2571-2_2576del
NM_145796.3:c.2286-2_2291del
NM_207171.2:c.2412-2_2417del
XM_005244999.1:c.2571-2_2576del
XM_005245000.3:c.2571-2_2576del
XM_005245001.1:c.2571-2_2576del
XM_005245005.1:c.2412-2_2417del
XM_005245006.3:c.2412-2_2417del
XM_011509330.1:c.2463-2_2468del
XM_011509331.1:c.2214-2_2219del
XR_921760.1:n.2399-2_2404del
XM_005244999.3:c.2571-2_2576del
XM_005245000.4:c.2571-2_2576del
XM_005245001.2:c.2571-2_2576del
XM_005245005.2:c.2412-2_2417del
XM_005245006.5:c.2412-2_2417del
XM_017000744.1:c.2592-2_2597del
XM_017000745.2:c.2544-2_2549del
XM_017000746.1:c.2544-2_2549del
XM_017000748.1:c.2412-2_2417del
XM_017000749.1:c.2412-2_2417del
XM_024454305.1:c.2445-2_2450del
XM_024454306.1:c.1371-2_1376del
XR_002959801.1:n.2426-2_2431del
NM_015100.4:c.2571-2_2576del
NM_001194937.2:c.2544-2_2549del
NM_001194938.2:c.2385-2_2390del
NM_145796.4:c.2286-2_2291del