Canonical Allele Identifier: CA891834765

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960931_87960932delinsCT , CM000672.2:g.87960931_87960932delinsCT	GRCh38
NC_000010.10:g.89720688_89720689delinsCT , CM000672.1:g.89720688_89720689delinsCT	GRCh37
NC_000010.9:g.89710668_89710669delinsCT	NCBI36
NG_007466.2:g.102493_102494delinsCT , LRG_311:g.102493_102494delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.932_933delinsCT	ENSP00000514759.2:p.Ile311Thr
ENST00000710265.1:c.839_840delinsCT	ENSP00000518161.1:p.Ile280Thr
ENST00000472832.3:c.839_840delinsCT	ENSP00000483066.2:p.Ile280Thr
ENST00000688158.2:n.1574_1575delinsCT
ENST00000688922.2:c.*669_*670delinsCT	ENSP00000508742.2:n.*669_*670delinsCT
ENST00000700021.1:c.794_795delinsCT	ENSP00000514757.1:p.Ile265Thr
ENST00000700022.1:c.*178_*179delinsCT	ENSP00000514758.1:n.*178_*179delinsCT
ENST00000700023.1:n.1997_1998delinsCT
ENST00000700024.1:n.2231_2232delinsCT
ENST00000700025.1:n.1608_1609delinsCT
ENST00000700026.1:n.476_477delinsCT
ENST00000700029.1:c.766_767delinsCT
ENST00000706954.1:c.839_840delinsCT	ENSP00000516674.1:p.Ile280Thr
ENST00000706955.1:c.*874_*875delinsCT	ENSP00000516675.1:n.*874_*875delinsCT
ENST00000686459.1:c.*425_*426delinsCT	ENSP00000508909.1:n.*425_*426delinsCT
ENST00000688158.1:c.*950_*951delinsCT	ENSP00000509254.1:n.*950_*951delinsCT
ENST00000688308.1:c.839_840delinsCT	ENSP00000508752.1:p.Ile280Thr
ENST00000688922.1:c.760_761delinsCT
ENST00000693560.1:c.1358_1359delinsCT	ENSP00000509861.1:p.Ile453Thr
ENST00000371953.8:c.839_840delinsCT MANE Select	ENSP00000361021.3:p.Ile280Thr
ENST00000371953.7:c.839_840delinsCT	ENSP00000361021.3:p.Ile280Thr
ENST00000472832.2:c.266_267delinsCT	ENSP00000483066.1:p.Ile89Thr
NM_000314.5:c.839_840delinsCT	NP_000305.3:p.Ile280Thr
NM_000314.6:c.839_840delinsCT	NP_000305.3:p.Ile280Thr
NM_001304717.2:c.1358_1359delinsCT	NP_001291646.2:p.Ile453Thr
NM_001304718.1:c.248_249delinsCT	NP_001291647.1:p.Ile83Thr
XM_006717926.2:c.794_795delinsCT	XP_006717989.1:p.Ile265Thr
XM_011539981.1:c.839_840delinsCT	XP_011538283.1:p.Ile280Thr
XM_011539982.1:c.743_744delinsCT	XP_011538284.1:p.Ile248Thr
XR_945791.1:n.1409_1410delinsCT
NM_000314.7:c.839_840delinsCT	NP_000305.3:p.Ile280Thr
NM_001304717.5:c.1358_1359delinsCT	NP_001291646.4:p.Ile453Thr
NM_001304718.2:c.248_249delinsCT	NP_001291647.1:p.Ile83Thr
NM_000314.8:c.839_840delinsCT MANE Select	NP_000305.3:p.Ile280Thr