Canonical Allele Identifier: CA341948621

Gene: POGZ

Linked Data

• MyVariant Identifiers: chr1:g.151378699C>A (hg19) ; chr1:g.151406223C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151406223C>A , CM000663.2:g.151406223C>A	GRCh38
NC_000001.10:g.151378699C>A , CM000663.1:g.151378699C>A	GRCh37
NC_000001.9:g.149645323C>A	NCBI36
NG_046601.1:g.58243G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.2860G>T	ENSP00000518163.1:p.Glu954Ter
ENST00000392723.6:c.2653G>T	ENSP00000376484.1:p.Glu885Ter
ENST00000439756.2:c.2812G>T	ENSP00000390156.2:p.Glu938Ter
ENST00000703168.1:c.2833G>T	ENSP00000515214.1:p.Glu945Ter
ENST00000271715.7:c.2812G>T MANE Select	ENSP00000271715.2:p.Glu938Ter
ENST00000271715.6:c.2812G>T	ENSP00000271715.2:p.Glu938Ter
ENST00000358476.7:n.2960G>T
ENST00000368863.6:c.2527G>T	ENSP00000357856.2:p.Glu843Ter
ENST00000392723.5:c.2653G>T	ENSP00000376484.1:p.Glu885Ter
ENST00000409503.5:c.2785G>T	ENSP00000386836.1:p.Glu929Ter
ENST00000491586.5:c.2680G>T	ENSP00000418408.1:p.Glu894Ter
ENST00000531094.5:c.2626G>T	ENSP00000431259.1:p.Glu876Ter
NM_001194937.1:c.2785G>T	NP_001181866.1:p.Glu929Ter
NM_001194938.1:c.2626G>T	NP_001181867.1:p.Glu876Ter
NM_015100.3:c.2812G>T	NP_055915.2:p.Glu938Ter
NM_145796.3:c.2527G>T	NP_665739.3:p.Glu843Ter
NM_207171.2:c.2653G>T	NP_997054.1:p.Glu885Ter
XM_005244999.1:c.2812G>T	XP_005245056.1:p.Glu938Ter
XM_005245000.3:c.2812G>T	XP_005245057.1:p.Glu938Ter
XM_005245001.1:c.2812G>T	XP_005245058.1:p.Glu938Ter
XM_005245005.1:c.2653G>T	XP_005245062.1:p.Glu885Ter
XM_005245006.3:c.2653G>T	XP_005245063.1:p.Glu885Ter
XM_011509330.1:c.2704G>T	XP_011507632.1:p.Glu902Ter
XM_011509331.1:c.2455G>T	XP_011507633.1:p.Glu819Ter
XM_005244999.3:c.2812G>T	XP_005245056.1:p.Glu938Ter
XM_005245000.4:c.2812G>T	XP_005245057.1:p.Glu938Ter
XM_005245001.2:c.2812G>T	XP_005245058.1:p.Glu938Ter
XM_005245005.2:c.2653G>T	XP_005245062.1:p.Glu885Ter
XM_005245006.5:c.2653G>T	XP_005245063.1:p.Glu885Ter
XM_017000744.1:c.2833G>T	XP_016856233.1:p.Glu945Ter
XM_017000745.2:c.2785G>T	XP_016856234.1:p.Glu929Ter
XM_017000746.1:c.2785G>T	XP_016856235.1:p.Glu929Ter
XM_017000748.1:c.2653G>T	XP_016856237.1:p.Glu885Ter
XM_017000749.1:c.2653G>T	XP_016856238.1:p.Glu885Ter
XM_024454305.1:c.2686G>T	XP_024310073.1:p.Glu896Ter
XM_024454306.1:c.1612G>T	XP_024310074.1:p.Glu538Ter
XR_002959801.1:n.2667G>T
NM_015100.4:c.2812G>T MANE Select	NP_055915.2:p.Glu938Ter
NM_001194937.2:c.2785G>T	NP_001181866.1:p.Glu929Ter
NM_001194938.2:c.2626G>T	NP_001181867.1:p.Glu876Ter
NM_145796.4:c.2527G>T	NP_665739.3:p.Glu843Ter