Canonical Allele Identifier: CA341944682

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378283C>G (hg19) ; chr1:g.151405807C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151405807C>G , CM000663.2:g.151405807C>G	GRCh38
NC_000001.10:g.151378283C>G , CM000663.1:g.151378283C>G	GRCh37
NC_000001.9:g.149644907C>G	NCBI36
NG_046601.1:g.58659G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.3276G>C	ENSP00000518163.1:p.Met1092Ile
ENST00000392723.6:c.3069G>C	ENSP00000376484.1:p.Met1023Ile
ENST00000439756.2:c.3228G>C	ENSP00000390156.2:p.Met1076Ile
ENST00000703168.1:c.3249G>C	ENSP00000515214.1:p.Met1083Ile
ENST00000271715.7:c.3228G>C MANE Select	ENSP00000271715.2:p.Met1076Ile
ENST00000271715.6:c.3228G>C	ENSP00000271715.2:p.Met1076Ile
ENST00000358476.7:n.3376G>C
ENST00000368863.6:c.2943G>C	ENSP00000357856.2:p.Met981Ile
ENST00000392723.5:c.3069G>C	ENSP00000376484.1:p.Met1023Ile
ENST00000409503.5:c.3201G>C	ENSP00000386836.1:p.Met1067Ile
ENST00000491586.5:c.3096G>C	ENSP00000418408.1:p.Met1032Ile
ENST00000531094.5:c.3042G>C	ENSP00000431259.1:p.Met1014Ile
NM_001194937.1:c.3201G>C	NP_001181866.1:p.Met1067Ile
NM_001194938.1:c.3042G>C	NP_001181867.1:p.Met1014Ile
NM_015100.3:c.3228G>C	NP_055915.2:p.Met1076Ile
NM_145796.3:c.2943G>C	NP_665739.3:p.Met981Ile
NM_207171.2:c.3069G>C	NP_997054.1:p.Met1023Ile
XM_005244999.1:c.3228G>C	XP_005245056.1:p.Met1076Ile
XM_005245000.3:c.3228G>C	XP_005245057.1:p.Met1076Ile
XM_005245001.1:c.3228G>C	XP_005245058.1:p.Met1076Ile
XM_005245005.1:c.3069G>C	XP_005245062.1:p.Met1023Ile
XM_005245006.3:c.3069G>C	XP_005245063.1:p.Met1023Ile
XM_011509330.1:c.3120G>C	XP_011507632.1:p.Met1040Ile
XM_011509331.1:c.2871G>C	XP_011507633.1:p.Met957Ile
XM_005244999.3:c.3228G>C	XP_005245056.1:p.Met1076Ile
XM_005245000.4:c.3228G>C	XP_005245057.1:p.Met1076Ile
XM_005245001.2:c.3228G>C	XP_005245058.1:p.Met1076Ile
XM_005245005.2:c.3069G>C	XP_005245062.1:p.Met1023Ile
XM_005245006.5:c.3069G>C	XP_005245063.1:p.Met1023Ile
XM_017000744.1:c.3249G>C	XP_016856233.1:p.Met1083Ile
XM_017000745.2:c.3201G>C	XP_016856234.1:p.Met1067Ile
XM_017000746.1:c.3201G>C	XP_016856235.1:p.Met1067Ile
XM_017000748.1:c.3069G>C	XP_016856237.1:p.Met1023Ile
XM_017000749.1:c.3069G>C	XP_016856238.1:p.Met1023Ile
XM_024454305.1:c.3102G>C	XP_024310073.1:p.Met1034Ile
XM_024454306.1:c.2028G>C	XP_024310074.1:p.Met676Ile
XR_002959801.1:n.3083G>C
NM_015100.4:c.3228G>C MANE Select	NP_055915.2:p.Met1076Ile
NM_001194937.2:c.3201G>C	NP_001181866.1:p.Met1067Ile
NM_001194938.2:c.3042G>C	NP_001181867.1:p.Met1014Ile
NM_145796.4:c.2943G>C	NP_665739.3:p.Met981Ile