Canonical Allele Identifier: CA2479578840

Gene: POGZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.151424958_151424960delinsCAT , CM000663.2:g.151424958_151424960delinsCAT	GRCh38
NC_000001.10:g.151397434_151397436delinsCAT , CM000663.1:g.151397434_151397436delinsCAT	GRCh37
NC_000001.9:g.149664058_149664060delinsCAT	NCBI36
NG_046601.1:g.39506_39508delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000710270.1:c.1228_1230delinsATG	ENSP00000518163.1:p.Met410=
ENST00000392723.6:c.1021_1023delinsATG	ENSP00000376484.1:p.Met341=
ENST00000439756.2:c.1180_1182delinsATG	ENSP00000390156.2:p.Met394=
ENST00000703168.1:c.1201_1203delinsATG	ENSP00000515214.1:p.Met401=
ENST00000703169.1:c.1153_1155delinsATG	ENSP00000515215.1:p.Met385=
ENST00000271715.7:c.1180_1182delinsATG MANE Select	ENSP00000271715.2:p.Met394=
ENST00000271715.6:c.1180_1182delinsATG	ENSP00000271715.2:p.Met394=
ENST00000358476.7:n.1049_1051delinsATG
ENST00000368863.6:c.895_897delinsATG	ENSP00000357856.2:p.Met299=
ENST00000392723.5:c.1021_1023delinsATG	ENSP00000376484.1:p.Met341=
ENST00000409503.5:c.1153_1155delinsATG	ENSP00000386836.1:p.Met385=
ENST00000441516.1:c.159-674_159-672delinsATG
ENST00000491586.5:c.1021_1023delinsATG	ENSP00000418408.1:p.Met341=
ENST00000495253.1:n.335_337delinsATG
ENST00000531094.5:c.994_996delinsATG	ENSP00000431259.1:p.Met332=
NM_001194937.1:c.1153_1155delinsATG	NP_001181866.1:p.Met385=
NM_001194938.1:c.994_996delinsATG	NP_001181867.1:p.Met332=
NM_015100.3:c.1180_1182delinsATG	NP_055915.2:p.Met394=
NM_145796.3:c.895_897delinsATG	NP_665739.3:p.Met299=
NM_207171.2:c.1021_1023delinsATG	NP_997054.1:p.Met341=
XM_005244999.1:c.1180_1182delinsATG	XP_005245056.1:p.Met394=
XM_005245000.3:c.1180_1182delinsATG	XP_005245057.1:p.Met394=
XM_005245001.1:c.1180_1182delinsATG	XP_005245058.1:p.Met394=
XM_005245005.1:c.1021_1023delinsATG	XP_005245062.1:p.Met341=
XM_005245006.3:c.1021_1023delinsATG	XP_005245063.1:p.Met341=
XM_011509330.1:c.1072_1074delinsATG	XP_011507632.1:p.Met358=
XM_011509331.1:c.823_825delinsATG	XP_011507633.1:p.Met275=
XR_921760.1:n.1181_1183delinsATG
XM_005244999.3:c.1180_1182delinsATG	XP_005245056.1:p.Met394=
XM_005245000.4:c.1180_1182delinsATG	XP_005245057.1:p.Met394=
XM_005245001.2:c.1180_1182delinsATG	XP_005245058.1:p.Met394=
XM_005245005.2:c.1021_1023delinsATG	XP_005245062.1:p.Met341=
XM_005245006.5:c.1021_1023delinsATG	XP_005245063.1:p.Met341=
XM_017000744.1:c.1201_1203delinsATG	XP_016856233.1:p.Met401=
XM_017000745.2:c.1153_1155delinsATG	XP_016856234.1:p.Met385=
XM_017000746.1:c.1153_1155delinsATG	XP_016856235.1:p.Met385=
XM_017000748.1:c.1021_1023delinsATG	XP_016856237.1:p.Met341=
XM_017000749.1:c.1021_1023delinsATG	XP_016856238.1:p.Met341=
XM_024454305.1:c.1201_1203delinsATG	XP_024310073.1:p.Met401=
XM_024454306.1:c.-15-674_-15-672delinsATG	XP_024310074.1:n.-15-674_-15-672delinsATG
XR_002959801.1:n.1208_1210delinsATG
NM_015100.4:c.1180_1182delinsATG MANE Select	NP_055915.2:p.Met394=
NM_001194937.2:c.1153_1155delinsATG	NP_001181866.1:p.Met385=
NM_001194938.2:c.994_996delinsATG	NP_001181867.1:p.Met332=
NM_145796.4:c.895_897delinsATG	NP_665739.3:p.Met299=