Canonical Allele Identifier: CA341949867

Gene: POGZ

Linked Data

• dbSNP Id: rs1392160287
• gnomAD v3: 1-151406403-AAGG-A
• gnomAD v4: 1-151406403-AAGG-A
• MyVariant Identifiers: chr1:g.151378880_151378882del (hg19) ; chr1:g.151406405_151406407del (hg38) ; chr1:g.151406404_151406406del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406410_151406412del , CM000663.2:g.151406410_151406412del	GRCh38
NC_000001.10:g.151378886_151378888del , CM000663.1:g.151378886_151378888del	GRCh37
NC_000001.9:g.149645510_149645512del	NCBI36
NG_046601.1:g.58060_58062del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2677_2679del	ENSP00000518163.1:p.Pro893del
ENST00000392723.6:c.2470_2472del	ENSP00000376484.1:p.Pro824del
ENST00000439756.2:c.2629_2631del	ENSP00000390156.2:p.Pro877del
ENST00000703168.1:c.2650_2652del	ENSP00000515214.1:p.Pro884del
ENST00000271715.7:c.2629_2631del MANE Select	ENSP00000271715.2:p.Pro877del
ENST00000271715.6:c.2629_2631del	ENSP00000271715.2:p.Pro877del
ENST00000358476.7:n.2777_2779del
ENST00000368863.6:c.2344_2346del	ENSP00000357856.2:p.Pro782del
ENST00000392723.5:c.2470_2472del	ENSP00000376484.1:p.Pro824del
ENST00000409503.5:c.2602_2604del	ENSP00000386836.1:p.Pro868del
ENST00000491586.5:c.2497_2499del	ENSP00000418408.1:p.Pro833del
ENST00000529669.1:c.829_831del	ENSP00000432295.1:p.Pro277del
ENST00000531094.5:c.2443_2445del	ENSP00000431259.1:p.Pro815del
NM_001194937.1:c.2602_2604del	NP_001181866.1:p.Pro868del
NM_001194938.1:c.2443_2445del	NP_001181867.1:p.Pro815del
NM_015100.3:c.2629_2631del	NP_055915.2:p.Pro877del
NM_145796.3:c.2344_2346del	NP_665739.3:p.Pro782del
NM_207171.2:c.2470_2472del	NP_997054.1:p.Pro824del
XM_005244999.1:c.2629_2631del	XP_005245056.1:p.Pro877del
XM_005245000.3:c.2629_2631del	XP_005245057.1:p.Pro877del
XM_005245001.1:c.2629_2631del	XP_005245058.1:p.Pro877del
XM_005245005.1:c.2470_2472del	XP_005245062.1:p.Pro824del
XM_005245006.3:c.2470_2472del	XP_005245063.1:p.Pro824del
XM_011509330.1:c.2521_2523del	XP_011507632.1:p.Pro841del
XM_011509331.1:c.2272_2274del	XP_011507633.1:p.Pro758del
XR_921760.1:n.2457_2459del
XM_005244999.3:c.2629_2631del	XP_005245056.1:p.Pro877del
XM_005245000.4:c.2629_2631del	XP_005245057.1:p.Pro877del
XM_005245001.2:c.2629_2631del	XP_005245058.1:p.Pro877del
XM_005245005.2:c.2470_2472del	XP_005245062.1:p.Pro824del
XM_005245006.5:c.2470_2472del	XP_005245063.1:p.Pro824del
XM_017000744.1:c.2650_2652del	XP_016856233.1:p.Pro884del
XM_017000745.2:c.2602_2604del	XP_016856234.1:p.Pro868del
XM_017000746.1:c.2602_2604del	XP_016856235.1:p.Pro868del
XM_017000748.1:c.2470_2472del	XP_016856237.1:p.Pro824del
XM_017000749.1:c.2470_2472del	XP_016856238.1:p.Pro824del
XM_024454305.1:c.2503_2505del	XP_024310073.1:p.Pro835del
XM_024454306.1:c.1429_1431del	XP_024310074.1:p.Pro477del
XR_002959801.1:n.2484_2486del
NM_015100.4:c.2629_2631del MANE Select	NP_055915.2:p.Pro877del
NM_001194937.2:c.2602_2604del	NP_001181866.1:p.Pro868del
NM_001194938.2:c.2443_2445del	NP_001181867.1:p.Pro815del
NM_145796.4:c.2344_2346del	NP_665739.3:p.Pro782del