Canonical Allele Identifier: CA341948420

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378680T>A (hg19) ; chr1:g.151406204T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406204T>A , CM000663.2:g.151406204T>A	GRCh38
NC_000001.10:g.151378680T>A , CM000663.1:g.151378680T>A	GRCh37
NC_000001.9:g.149645304T>A	NCBI36
NG_046601.1:g.58262A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2879A>T	ENSP00000518163.1:p.Asp960Val
ENST00000392723.6:c.2672A>T	ENSP00000376484.1:p.Asp891Val
ENST00000439756.2:c.2831A>T	ENSP00000390156.2:p.Asp944Val
ENST00000703168.1:c.2852A>T	ENSP00000515214.1:p.Asp951Val
ENST00000271715.7:c.2831A>T MANE Select	ENSP00000271715.2:p.Asp944Val
ENST00000271715.6:c.2831A>T	ENSP00000271715.2:p.Asp944Val
ENST00000358476.7:n.2979A>T
ENST00000368863.6:c.2546A>T	ENSP00000357856.2:p.Asp849Val
ENST00000392723.5:c.2672A>T	ENSP00000376484.1:p.Asp891Val
ENST00000409503.5:c.2804A>T	ENSP00000386836.1:p.Asp935Val
ENST00000491586.5:c.2699A>T	ENSP00000418408.1:p.Asp900Val
ENST00000531094.5:c.2645A>T	ENSP00000431259.1:p.Asp882Val
NM_001194937.1:c.2804A>T	NP_001181866.1:p.Asp935Val
NM_001194938.1:c.2645A>T	NP_001181867.1:p.Asp882Val
NM_015100.3:c.2831A>T	NP_055915.2:p.Asp944Val
NM_145796.3:c.2546A>T	NP_665739.3:p.Asp849Val
NM_207171.2:c.2672A>T	NP_997054.1:p.Asp891Val
XM_005244999.1:c.2831A>T	XP_005245056.1:p.Asp944Val
XM_005245000.3:c.2831A>T	XP_005245057.1:p.Asp944Val
XM_005245001.1:c.2831A>T	XP_005245058.1:p.Asp944Val
XM_005245005.1:c.2672A>T	XP_005245062.1:p.Asp891Val
XM_005245006.3:c.2672A>T	XP_005245063.1:p.Asp891Val
XM_011509330.1:c.2723A>T	XP_011507632.1:p.Asp908Val
XM_011509331.1:c.2474A>T	XP_011507633.1:p.Asp825Val
XM_005244999.3:c.2831A>T	XP_005245056.1:p.Asp944Val
XM_005245000.4:c.2831A>T	XP_005245057.1:p.Asp944Val
XM_005245001.2:c.2831A>T	XP_005245058.1:p.Asp944Val
XM_005245005.2:c.2672A>T	XP_005245062.1:p.Asp891Val
XM_005245006.5:c.2672A>T	XP_005245063.1:p.Asp891Val
XM_017000744.1:c.2852A>T	XP_016856233.1:p.Asp951Val
XM_017000745.2:c.2804A>T	XP_016856234.1:p.Asp935Val
XM_017000746.1:c.2804A>T	XP_016856235.1:p.Asp935Val
XM_017000748.1:c.2672A>T	XP_016856237.1:p.Asp891Val
XM_017000749.1:c.2672A>T	XP_016856238.1:p.Asp891Val
XM_024454305.1:c.2705A>T	XP_024310073.1:p.Asp902Val
XM_024454306.1:c.1631A>T	XP_024310074.1:p.Asp544Val
XR_002959801.1:n.2686A>T
NM_015100.4:c.2831A>T MANE Select	NP_055915.2:p.Asp944Val
NM_001194937.2:c.2804A>T	NP_001181866.1:p.Asp935Val
NM_001194938.2:c.2645A>T	NP_001181867.1:p.Asp882Val
NM_145796.4:c.2546A>T	NP_665739.3:p.Asp849Val