Canonical Allele Identifier: CA341949956

Gene: POGZ

Linked Data

• dbSNP Id: rs1653625441
• gnomAD v4: 1-151406417-A-G
• MyVariant Identifiers: chr1:g.151378893A>G (hg19) ; chr1:g.151406417A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406417A>G , CM000663.2:g.151406417A>G	GRCh38
NC_000001.10:g.151378893A>G , CM000663.1:g.151378893A>G	GRCh37
NC_000001.9:g.149645517A>G	NCBI36
NG_046601.1:g.58049T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2666T>C	ENSP00000518163.1:p.Met889Thr
ENST00000392723.6:c.2459T>C	ENSP00000376484.1:p.Met820Thr
ENST00000439756.2:c.2618T>C	ENSP00000390156.2:p.Met873Thr
ENST00000703168.1:c.2639T>C	ENSP00000515214.1:p.Met880Thr
ENST00000271715.7:c.2618T>C MANE Select	ENSP00000271715.2:p.Met873Thr
ENST00000271715.6:c.2618T>C	ENSP00000271715.2:p.Met873Thr
ENST00000358476.7:n.2766T>C
ENST00000368863.6:c.2333T>C	ENSP00000357856.2:p.Met778Thr
ENST00000392723.5:c.2459T>C	ENSP00000376484.1:p.Met820Thr
ENST00000409503.5:c.2591T>C	ENSP00000386836.1:p.Met864Thr
ENST00000491586.5:c.2486T>C	ENSP00000418408.1:p.Met829Thr
ENST00000529669.1:c.818T>C	ENSP00000432295.1:p.Met273Thr
ENST00000531094.5:c.2432T>C	ENSP00000431259.1:p.Met811Thr
NM_001194937.1:c.2591T>C	NP_001181866.1:p.Met864Thr
NM_001194938.1:c.2432T>C	NP_001181867.1:p.Met811Thr
NM_015100.3:c.2618T>C	NP_055915.2:p.Met873Thr
NM_145796.3:c.2333T>C	NP_665739.3:p.Met778Thr
NM_207171.2:c.2459T>C	NP_997054.1:p.Met820Thr
XM_005244999.1:c.2618T>C	XP_005245056.1:p.Met873Thr
XM_005245000.3:c.2618T>C	XP_005245057.1:p.Met873Thr
XM_005245001.1:c.2618T>C	XP_005245058.1:p.Met873Thr
XM_005245005.1:c.2459T>C	XP_005245062.1:p.Met820Thr
XM_005245006.3:c.2459T>C	XP_005245063.1:p.Met820Thr
XM_011509330.1:c.2510T>C	XP_011507632.1:p.Met837Thr
XM_011509331.1:c.2261T>C	XP_011507633.1:p.Met754Thr
XR_921760.1:n.2446T>C
XM_005244999.3:c.2618T>C	XP_005245056.1:p.Met873Thr
XM_005245000.4:c.2618T>C	XP_005245057.1:p.Met873Thr
XM_005245001.2:c.2618T>C	XP_005245058.1:p.Met873Thr
XM_005245005.2:c.2459T>C	XP_005245062.1:p.Met820Thr
XM_005245006.5:c.2459T>C	XP_005245063.1:p.Met820Thr
XM_017000744.1:c.2639T>C	XP_016856233.1:p.Met880Thr
XM_017000745.2:c.2591T>C	XP_016856234.1:p.Met864Thr
XM_017000746.1:c.2591T>C	XP_016856235.1:p.Met864Thr
XM_017000748.1:c.2459T>C	XP_016856237.1:p.Met820Thr
XM_017000749.1:c.2459T>C	XP_016856238.1:p.Met820Thr
XM_024454305.1:c.2492T>C	XP_024310073.1:p.Met831Thr
XM_024454306.1:c.1418T>C	XP_024310074.1:p.Met473Thr
XR_002959801.1:n.2473T>C
NM_015100.4:c.2618T>C MANE Select	NP_055915.2:p.Met873Thr
NM_001194937.2:c.2591T>C	NP_001181866.1:p.Met864Thr
NM_001194938.2:c.2432T>C	NP_001181867.1:p.Met811Thr
NM_145796.4:c.2333T>C	NP_665739.3:p.Met778Thr