Canonical Allele Identifier: CA341949645

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378849T>A (hg19) ; chr1:g.151406373T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406373T>A , CM000663.2:g.151406373T>A	GRCh38
NC_000001.10:g.151378849T>A , CM000663.1:g.151378849T>A	GRCh37
NC_000001.9:g.149645473T>A	NCBI36
NG_046601.1:g.58093A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2710A>T	ENSP00000518163.1:p.Lys904Ter
ENST00000392723.6:c.2503A>T	ENSP00000376484.1:p.Lys835Ter
ENST00000439756.2:c.2662A>T	ENSP00000390156.2:p.Lys888Ter
ENST00000703168.1:c.2683A>T	ENSP00000515214.1:p.Lys895Ter
ENST00000271715.7:c.2662A>T MANE Select	ENSP00000271715.2:p.Lys888Ter
ENST00000271715.6:c.2662A>T	ENSP00000271715.2:p.Lys888Ter
ENST00000358476.7:n.2810A>T
ENST00000368863.6:c.2377A>T	ENSP00000357856.2:p.Lys793Ter
ENST00000392723.5:c.2503A>T	ENSP00000376484.1:p.Lys835Ter
ENST00000409503.5:c.2635A>T	ENSP00000386836.1:p.Lys879Ter
ENST00000491586.5:c.2530A>T	ENSP00000418408.1:p.Lys844Ter
ENST00000529669.1:c.862A>T	ENSP00000432295.1:p.Lys288Ter
ENST00000531094.5:c.2476A>T	ENSP00000431259.1:p.Lys826Ter
NM_001194937.1:c.2635A>T	NP_001181866.1:p.Lys879Ter
NM_001194938.1:c.2476A>T	NP_001181867.1:p.Lys826Ter
NM_015100.3:c.2662A>T	NP_055915.2:p.Lys888Ter
NM_145796.3:c.2377A>T	NP_665739.3:p.Lys793Ter
NM_207171.2:c.2503A>T	NP_997054.1:p.Lys835Ter
XM_005244999.1:c.2662A>T	XP_005245056.1:p.Lys888Ter
XM_005245000.3:c.2662A>T	XP_005245057.1:p.Lys888Ter
XM_005245001.1:c.2662A>T	XP_005245058.1:p.Lys888Ter
XM_005245005.1:c.2503A>T	XP_005245062.1:p.Lys835Ter
XM_005245006.3:c.2503A>T	XP_005245063.1:p.Lys835Ter
XM_011509330.1:c.2554A>T	XP_011507632.1:p.Lys852Ter
XM_011509331.1:c.2305A>T	XP_011507633.1:p.Lys769Ter
XM_005244999.3:c.2662A>T	XP_005245056.1:p.Lys888Ter
XM_005245000.4:c.2662A>T	XP_005245057.1:p.Lys888Ter
XM_005245001.2:c.2662A>T	XP_005245058.1:p.Lys888Ter
XM_005245005.2:c.2503A>T	XP_005245062.1:p.Lys835Ter
XM_005245006.5:c.2503A>T	XP_005245063.1:p.Lys835Ter
XM_017000744.1:c.2683A>T	XP_016856233.1:p.Lys895Ter
XM_017000745.2:c.2635A>T	XP_016856234.1:p.Lys879Ter
XM_017000746.1:c.2635A>T	XP_016856235.1:p.Lys879Ter
XM_017000748.1:c.2503A>T	XP_016856237.1:p.Lys835Ter
XM_017000749.1:c.2503A>T	XP_016856238.1:p.Lys835Ter
XM_024454305.1:c.2536A>T	XP_024310073.1:p.Lys846Ter
XM_024454306.1:c.1462A>T	XP_024310074.1:p.Lys488Ter
XR_002959801.1:n.2517A>T
NM_015100.4:c.2662A>T MANE Select	NP_055915.2:p.Lys888Ter
NM_001194937.2:c.2635A>T	NP_001181866.1:p.Lys879Ter
NM_001194938.2:c.2476A>T	NP_001181867.1:p.Lys826Ter
NM_145796.4:c.2377A>T	NP_665739.3:p.Lys793Ter