Canonical Allele Identifier: CA420909653

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378826A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406350A>G , CM000663.2:g.151406350A>G	GRCh38
NC_000001.10:g.151378826A>G , CM000663.1:g.151378826A>G	GRCh37
NC_000001.9:g.149645450A>G	NCBI36
NG_046601.1:g.58116T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2733T>C	ENSP00000518163.1:p.Ala911=
ENST00000392723.6:c.2526T>C	ENSP00000376484.1:p.Ala842=
ENST00000439756.2:c.2685T>C	ENSP00000390156.2:p.Ala895=
ENST00000703168.1:c.2706T>C	ENSP00000515214.1:p.Ala902=
ENST00000271715.7:c.2685T>C MANE Select	ENSP00000271715.2:p.Ala895=
ENST00000271715.6:c.2685T>C	ENSP00000271715.2:p.Ala895=
ENST00000358476.7:n.2833T>C
ENST00000368863.6:c.2400T>C	ENSP00000357856.2:p.Ala800=
ENST00000392723.5:c.2526T>C	ENSP00000376484.1:p.Ala842=
ENST00000409503.5:c.2658T>C	ENSP00000386836.1:p.Ala886=
ENST00000491586.5:c.2553T>C	ENSP00000418408.1:p.Ala851=
ENST00000529669.1:c.885T>C	ENSP00000432295.1:p.Ala295=
ENST00000531094.5:c.2499T>C	ENSP00000431259.1:p.Ala833=
NM_001194937.1:c.2658T>C	NP_001181866.1:p.Ala886=
NM_001194938.1:c.2499T>C	NP_001181867.1:p.Ala833=
NM_015100.3:c.2685T>C	NP_055915.2:p.Ala895=
NM_145796.3:c.2400T>C	NP_665739.3:p.Ala800=
NM_207171.2:c.2526T>C	NP_997054.1:p.Ala842=
XM_005244999.1:c.2685T>C	XP_005245056.1:p.Ala895=
XM_005245000.3:c.2685T>C	XP_005245057.1:p.Ala895=
XM_005245001.1:c.2685T>C	XP_005245058.1:p.Ala895=
XM_005245005.1:c.2526T>C	XP_005245062.1:p.Ala842=
XM_005245006.3:c.2526T>C	XP_005245063.1:p.Ala842=
XM_011509330.1:c.2577T>C	XP_011507632.1:p.Ala859=
XM_011509331.1:c.2328T>C	XP_011507633.1:p.Ala776=
XM_005244999.3:c.2685T>C	XP_005245056.1:p.Ala895=
XM_005245000.4:c.2685T>C	XP_005245057.1:p.Ala895=
XM_005245001.2:c.2685T>C	XP_005245058.1:p.Ala895=
XM_005245005.2:c.2526T>C	XP_005245062.1:p.Ala842=
XM_005245006.5:c.2526T>C	XP_005245063.1:p.Ala842=
XM_017000744.1:c.2706T>C	XP_016856233.1:p.Ala902=
XM_017000745.2:c.2658T>C	XP_016856234.1:p.Ala886=
XM_017000746.1:c.2658T>C	XP_016856235.1:p.Ala886=
XM_017000748.1:c.2526T>C	XP_016856237.1:p.Ala842=
XM_017000749.1:c.2526T>C	XP_016856238.1:p.Ala842=
XM_024454305.1:c.2559T>C	XP_024310073.1:p.Ala853=
XM_024454306.1:c.1485T>C	XP_024310074.1:p.Ala495=
XR_002959801.1:n.2540T>C
NM_015100.4:c.2685T>C MANE Select	NP_055915.2:p.Ala895=
NM_001194937.2:c.2658T>C	NP_001181866.1:p.Ala886=
NM_001194938.2:c.2499T>C	NP_001181867.1:p.Ala833=
NM_145796.4:c.2400T>C	NP_665739.3:p.Ala800=