Canonical Allele Identifier: CA341950247

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378936C>G (hg19) ; chr1:g.151406460C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406460C>G , CM000663.2:g.151406460C>G	GRCh38
NC_000001.10:g.151378936C>G , CM000663.1:g.151378936C>G	GRCh37
NC_000001.9:g.149645560C>G	NCBI36
NG_046601.1:g.58006G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2623G>C	ENSP00000518163.1:p.Gly875Arg
ENST00000392723.6:c.2416G>C	ENSP00000376484.1:p.Gly806Arg
ENST00000439756.2:c.2575G>C	ENSP00000390156.2:p.Gly859Arg
ENST00000703168.1:c.2596G>C	ENSP00000515214.1:p.Gly866Arg
ENST00000271715.7:c.2575G>C MANE Select	ENSP00000271715.2:p.Gly859Arg
ENST00000271715.6:c.2575G>C	ENSP00000271715.2:p.Gly859Arg
ENST00000358476.7:n.2723G>C
ENST00000368863.6:c.2290G>C	ENSP00000357856.2:p.Gly764Arg
ENST00000392723.5:c.2416G>C	ENSP00000376484.1:p.Gly806Arg
ENST00000409503.5:c.2548G>C	ENSP00000386836.1:p.Gly850Arg
ENST00000491586.5:c.2443G>C	ENSP00000418408.1:p.Gly815Arg
ENST00000529669.1:c.775G>C	ENSP00000432295.1:p.Gly259Arg
ENST00000531094.5:c.2389G>C	ENSP00000431259.1:p.Gly797Arg
NM_001194937.1:c.2548G>C	NP_001181866.1:p.Gly850Arg
NM_001194938.1:c.2389G>C	NP_001181867.1:p.Gly797Arg
NM_015100.3:c.2575G>C	NP_055915.2:p.Gly859Arg
NM_145796.3:c.2290G>C	NP_665739.3:p.Gly764Arg
NM_207171.2:c.2416G>C	NP_997054.1:p.Gly806Arg
XM_005244999.1:c.2575G>C	XP_005245056.1:p.Gly859Arg
XM_005245000.3:c.2575G>C	XP_005245057.1:p.Gly859Arg
XM_005245001.1:c.2575G>C	XP_005245058.1:p.Gly859Arg
XM_005245005.1:c.2416G>C	XP_005245062.1:p.Gly806Arg
XM_005245006.3:c.2416G>C	XP_005245063.1:p.Gly806Arg
XM_011509330.1:c.2467G>C	XP_011507632.1:p.Gly823Arg
XM_011509331.1:c.2218G>C	XP_011507633.1:p.Gly740Arg
XR_921760.1:n.2403G>C
XM_005244999.3:c.2575G>C	XP_005245056.1:p.Gly859Arg
XM_005245000.4:c.2575G>C	XP_005245057.1:p.Gly859Arg
XM_005245001.2:c.2575G>C	XP_005245058.1:p.Gly859Arg
XM_005245005.2:c.2416G>C	XP_005245062.1:p.Gly806Arg
XM_005245006.5:c.2416G>C	XP_005245063.1:p.Gly806Arg
XM_017000744.1:c.2596G>C	XP_016856233.1:p.Gly866Arg
XM_017000745.2:c.2548G>C	XP_016856234.1:p.Gly850Arg
XM_017000746.1:c.2548G>C	XP_016856235.1:p.Gly850Arg
XM_017000748.1:c.2416G>C	XP_016856237.1:p.Gly806Arg
XM_017000749.1:c.2416G>C	XP_016856238.1:p.Gly806Arg
XM_024454305.1:c.2449G>C	XP_024310073.1:p.Gly817Arg
XM_024454306.1:c.1375G>C	XP_024310074.1:p.Gly459Arg
XR_002959801.1:n.2430G>C
NM_015100.4:c.2575G>C MANE Select	NP_055915.2:p.Gly859Arg
NM_001194937.2:c.2548G>C	NP_001181866.1:p.Gly850Arg
NM_001194938.2:c.2389G>C	NP_001181867.1:p.Gly797Arg
NM_145796.4:c.2290G>C	NP_665739.3:p.Gly764Arg