Canonical Allele Identifier: CA341956378

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151380931A>G (hg19) ; chr1:g.151408455A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151408455A>G , CM000663.2:g.151408455A>G	GRCh38
NC_000001.10:g.151380931A>G , CM000663.1:g.151380931A>G	GRCh37
NC_000001.9:g.149647555A>G	NCBI36
NG_046601.1:g.56011T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000710270.1:c.2236T>C	ENSP00000518163.1:p.Tyr746His
ENST00000392723.6:c.2029T>C	ENSP00000376484.1:p.Tyr677His
ENST00000439756.2:c.2188T>C	ENSP00000390156.2:p.Tyr730His
ENST00000703168.1:c.2209T>C	ENSP00000515214.1:p.Tyr737His
ENST00000271715.7:c.2188T>C MANE Select	ENSP00000271715.2:p.Tyr730His
ENST00000271715.6:c.2188T>C	ENSP00000271715.2:p.Tyr730His
ENST00000358476.7:n.2057T>C
ENST00000368863.6:c.1903T>C	ENSP00000357856.2:p.Tyr635His
ENST00000392723.5:c.2029T>C	ENSP00000376484.1:p.Tyr677His
ENST00000409503.5:c.2161T>C	ENSP00000386836.1:p.Tyr721His
ENST00000491586.5:c.2056T>C	ENSP00000418408.1:p.Tyr686His
ENST00000492528.1:n.99T>C
ENST00000529669.1:c.388T>C	ENSP00000432295.1:p.Tyr130His
ENST00000531094.5:c.2002T>C	ENSP00000431259.1:p.Tyr668His
NM_001194937.1:c.2161T>C	NP_001181866.1:p.Tyr721His
NM_001194938.1:c.2002T>C	NP_001181867.1:p.Tyr668His
NM_015100.3:c.2188T>C	NP_055915.2:p.Tyr730His
NM_145796.3:c.1903T>C	NP_665739.3:p.Tyr635His
NM_207171.2:c.2029T>C	NP_997054.1:p.Tyr677His
XM_005244999.1:c.2188T>C	XP_005245056.1:p.Tyr730His
XM_005245000.3:c.2188T>C	XP_005245057.1:p.Tyr730His
XM_005245001.1:c.2188T>C	XP_005245058.1:p.Tyr730His
XM_005245005.1:c.2029T>C	XP_005245062.1:p.Tyr677His
XM_005245006.3:c.2029T>C	XP_005245063.1:p.Tyr677His
XM_011509330.1:c.2080T>C	XP_011507632.1:p.Tyr694His
XM_011509331.1:c.1831T>C	XP_011507633.1:p.Tyr611His
XR_921760.1:n.2063-215T>C
XM_005244999.3:c.2188T>C	XP_005245056.1:p.Tyr730His
XM_005245000.4:c.2188T>C	XP_005245057.1:p.Tyr730His
XM_005245001.2:c.2188T>C	XP_005245058.1:p.Tyr730His
XM_005245005.2:c.2029T>C	XP_005245062.1:p.Tyr677His
XM_005245006.5:c.2029T>C	XP_005245063.1:p.Tyr677His
XM_017000744.1:c.2209T>C	XP_016856233.1:p.Tyr737His
XM_017000745.2:c.2161T>C	XP_016856234.1:p.Tyr721His
XM_017000746.1:c.2161T>C	XP_016856235.1:p.Tyr721His
XM_017000748.1:c.2029T>C	XP_016856237.1:p.Tyr677His
XM_017000749.1:c.2029T>C	XP_016856238.1:p.Tyr677His
XM_024454305.1:c.2062T>C	XP_024310073.1:p.Tyr688His
XM_024454306.1:c.988T>C	XP_024310074.1:p.Tyr330His
XR_002959801.1:n.2090-215T>C
NM_015100.4:c.2188T>C MANE Select	NP_055915.2:p.Tyr730His
NM_001194937.2:c.2161T>C	NP_001181866.1:p.Tyr721His
NM_001194938.2:c.2002T>C	NP_001181867.1:p.Tyr668His
NM_145796.4:c.1903T>C	NP_665739.3:p.Tyr635His