Canonical Allele Identifier: CA341950140

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378914T>G (hg19) ; chr1:g.151406438T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406438T>G , CM000663.2:g.151406438T>G	GRCh38
NC_000001.10:g.151378914T>G , CM000663.1:g.151378914T>G	GRCh37
NC_000001.9:g.149645538T>G	NCBI36
NG_046601.1:g.58028A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2645A>C	ENSP00000518163.1:p.His882Pro
ENST00000392723.6:c.2438A>C	ENSP00000376484.1:p.His813Pro
ENST00000439756.2:c.2597A>C	ENSP00000390156.2:p.His866Pro
ENST00000703168.1:c.2618A>C	ENSP00000515214.1:p.His873Pro
ENST00000271715.7:c.2597A>C MANE Select	ENSP00000271715.2:p.His866Pro
ENST00000271715.6:c.2597A>C	ENSP00000271715.2:p.His866Pro
ENST00000358476.7:n.2745A>C
ENST00000368863.6:c.2312A>C	ENSP00000357856.2:p.His771Pro
ENST00000392723.5:c.2438A>C	ENSP00000376484.1:p.His813Pro
ENST00000409503.5:c.2570A>C	ENSP00000386836.1:p.His857Pro
ENST00000491586.5:c.2465A>C	ENSP00000418408.1:p.His822Pro
ENST00000529669.1:c.797A>C	ENSP00000432295.1:p.His266Pro
ENST00000531094.5:c.2411A>C	ENSP00000431259.1:p.His804Pro
NM_001194937.1:c.2570A>C	NP_001181866.1:p.His857Pro
NM_001194938.1:c.2411A>C	NP_001181867.1:p.His804Pro
NM_015100.3:c.2597A>C	NP_055915.2:p.His866Pro
NM_145796.3:c.2312A>C	NP_665739.3:p.His771Pro
NM_207171.2:c.2438A>C	NP_997054.1:p.His813Pro
XM_005244999.1:c.2597A>C	XP_005245056.1:p.His866Pro
XM_005245000.3:c.2597A>C	XP_005245057.1:p.His866Pro
XM_005245001.1:c.2597A>C	XP_005245058.1:p.His866Pro
XM_005245005.1:c.2438A>C	XP_005245062.1:p.His813Pro
XM_005245006.3:c.2438A>C	XP_005245063.1:p.His813Pro
XM_011509330.1:c.2489A>C	XP_011507632.1:p.His830Pro
XM_011509331.1:c.2240A>C	XP_011507633.1:p.His747Pro
XR_921760.1:n.2425A>C
XM_005244999.3:c.2597A>C	XP_005245056.1:p.His866Pro
XM_005245000.4:c.2597A>C	XP_005245057.1:p.His866Pro
XM_005245001.2:c.2597A>C	XP_005245058.1:p.His866Pro
XM_005245005.2:c.2438A>C	XP_005245062.1:p.His813Pro
XM_005245006.5:c.2438A>C	XP_005245063.1:p.His813Pro
XM_017000744.1:c.2618A>C	XP_016856233.1:p.His873Pro
XM_017000745.2:c.2570A>C	XP_016856234.1:p.His857Pro
XM_017000746.1:c.2570A>C	XP_016856235.1:p.His857Pro
XM_017000748.1:c.2438A>C	XP_016856237.1:p.His813Pro
XM_017000749.1:c.2438A>C	XP_016856238.1:p.His813Pro
XM_024454305.1:c.2471A>C	XP_024310073.1:p.His824Pro
XM_024454306.1:c.1397A>C	XP_024310074.1:p.His466Pro
XR_002959801.1:n.2452A>C
NM_015100.4:c.2597A>C MANE Select	NP_055915.2:p.His866Pro
NM_001194937.2:c.2570A>C	NP_001181866.1:p.His857Pro
NM_001194938.2:c.2411A>C	NP_001181867.1:p.His804Pro
NM_145796.4:c.2312A>C	NP_665739.3:p.His771Pro