Canonical Allele Identifier: CA341950231

Gene: POGZ

Linked Data

• dbSNP Id: rs1276204339
• gnomAD v3: 1-151406456-T-C
• gnomAD v4: 1-151406456-T-C
• MyVariant Identifiers: chr1:g.151378932T>C (hg19) ; chr1:g.151406456T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406456T>C , CM000663.2:g.151406456T>C	GRCh38
NC_000001.10:g.151378932T>C , CM000663.1:g.151378932T>C	GRCh37
NC_000001.9:g.149645556T>C	NCBI36
NG_046601.1:g.58010A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2627A>G	ENSP00000518163.1:p.Gln876Arg
ENST00000392723.6:c.2420A>G	ENSP00000376484.1:p.Gln807Arg
ENST00000439756.2:c.2579A>G	ENSP00000390156.2:p.Gln860Arg
ENST00000703168.1:c.2600A>G	ENSP00000515214.1:p.Gln867Arg
ENST00000271715.7:c.2579A>G MANE Select	ENSP00000271715.2:p.Gln860Arg
ENST00000271715.6:c.2579A>G	ENSP00000271715.2:p.Gln860Arg
ENST00000358476.7:n.2727A>G
ENST00000368863.6:c.2294A>G	ENSP00000357856.2:p.Gln765Arg
ENST00000392723.5:c.2420A>G	ENSP00000376484.1:p.Gln807Arg
ENST00000409503.5:c.2552A>G	ENSP00000386836.1:p.Gln851Arg
ENST00000491586.5:c.2447A>G	ENSP00000418408.1:p.Gln816Arg
ENST00000529669.1:c.779A>G	ENSP00000432295.1:p.Gln260Arg
ENST00000531094.5:c.2393A>G	ENSP00000431259.1:p.Gln798Arg
NM_001194937.1:c.2552A>G	NP_001181866.1:p.Gln851Arg
NM_001194938.1:c.2393A>G	NP_001181867.1:p.Gln798Arg
NM_015100.3:c.2579A>G	NP_055915.2:p.Gln860Arg
NM_145796.3:c.2294A>G	NP_665739.3:p.Gln765Arg
NM_207171.2:c.2420A>G	NP_997054.1:p.Gln807Arg
XM_005244999.1:c.2579A>G	XP_005245056.1:p.Gln860Arg
XM_005245000.3:c.2579A>G	XP_005245057.1:p.Gln860Arg
XM_005245001.1:c.2579A>G	XP_005245058.1:p.Gln860Arg
XM_005245005.1:c.2420A>G	XP_005245062.1:p.Gln807Arg
XM_005245006.3:c.2420A>G	XP_005245063.1:p.Gln807Arg
XM_011509330.1:c.2471A>G	XP_011507632.1:p.Gln824Arg
XM_011509331.1:c.2222A>G	XP_011507633.1:p.Gln741Arg
XR_921760.1:n.2407A>G
XM_005244999.3:c.2579A>G	XP_005245056.1:p.Gln860Arg
XM_005245000.4:c.2579A>G	XP_005245057.1:p.Gln860Arg
XM_005245001.2:c.2579A>G	XP_005245058.1:p.Gln860Arg
XM_005245005.2:c.2420A>G	XP_005245062.1:p.Gln807Arg
XM_005245006.5:c.2420A>G	XP_005245063.1:p.Gln807Arg
XM_017000744.1:c.2600A>G	XP_016856233.1:p.Gln867Arg
XM_017000745.2:c.2552A>G	XP_016856234.1:p.Gln851Arg
XM_017000746.1:c.2552A>G	XP_016856235.1:p.Gln851Arg
XM_017000748.1:c.2420A>G	XP_016856237.1:p.Gln807Arg
XM_017000749.1:c.2420A>G	XP_016856238.1:p.Gln807Arg
XM_024454305.1:c.2453A>G	XP_024310073.1:p.Gln818Arg
XM_024454306.1:c.1379A>G	XP_024310074.1:p.Gln460Arg
XR_002959801.1:n.2434A>G
NM_015100.4:c.2579A>G MANE Select	NP_055915.2:p.Gln860Arg
NM_001194937.2:c.2552A>G	NP_001181866.1:p.Gln851Arg
NM_001194938.2:c.2393A>G	NP_001181867.1:p.Gln798Arg
NM_145796.4:c.2294A>G	NP_665739.3:p.Gln765Arg