Canonical Allele Identifier: CA1926190084

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961054_87961055delinsCA , CM000672.2:g.87961054_87961055delinsCA	GRCh38
NC_000010.10:g.89720811_89720812delinsCA , CM000672.1:g.89720811_89720812delinsCA	GRCh37
NC_000010.9:g.89710791_89710792delinsCA	NCBI36
NG_007466.2:g.102616_102617delinsCA , LRG_311:g.102616_102617delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1055_1056delinsCA	ENSP00000514759.2:p.Thr352=
ENST00000710265.1:c.962_963delinsCA	ENSP00000518161.1:p.Thr321=
ENST00000472832.3:c.962_963delinsCA	ENSP00000483066.2:p.Thr321=
ENST00000688158.2:n.1697_1698delinsCA
ENST00000688922.2:c.*792_*793delinsCA	ENSP00000508742.2:n.*792_*793delinsCA
ENST00000700021.1:c.917_918delinsCA	ENSP00000514757.1:p.Thr306=
ENST00000700022.1:c.*301_*302delinsCA	ENSP00000514758.1:n.*301_*302delinsCA
ENST00000700023.1:n.2120_2121delinsCA
ENST00000700024.1:n.2354_2355delinsCA
ENST00000700025.1:n.1731_1732delinsCA
ENST00000700026.1:n.599_600delinsCA
ENST00000706954.1:c.962_963delinsCA	ENSP00000516674.1:p.Thr321=
ENST00000706955.1:c.*997_*998delinsCA	ENSP00000516675.1:n.*997_*998delinsCA
ENST00000686459.1:c.*548_*549delinsCA	ENSP00000508909.1:n.*548_*549delinsCA
ENST00000688158.1:c.*1073_*1074delinsCA	ENSP00000509254.1:n.*1073_*1074delinsCA
ENST00000688308.1:c.962_963delinsCA	ENSP00000508752.1:p.Thr321=
ENST00000688922.1:c.883_884delinsCA
ENST00000693560.1:c.1481_1482delinsCA	ENSP00000509861.1:p.Thr494=
ENST00000371953.8:c.962_963delinsCA MANE Select	ENSP00000361021.3:p.Thr321=
ENST00000371953.7:c.962_963delinsCA	ENSP00000361021.3:p.Thr321=
ENST00000472832.2:c.389_390delinsCA	ENSP00000483066.1:p.Thr130=
NM_000314.5:c.962_963delinsCA	NP_000305.3:p.Thr321=
NM_000314.6:c.962_963delinsCA	NP_000305.3:p.Thr321=
NM_001304717.2:c.1481_1482delinsCA	NP_001291646.2:p.Thr494=
NM_001304718.1:c.371_372delinsCA	NP_001291647.1:p.Thr124=
XM_006717926.2:c.917_918delinsCA	XP_006717989.1:p.Thr306=
XM_011539981.1:c.962_963delinsCA	XP_011538283.1:p.Thr321=
XM_011539982.1:c.866_867delinsCA	XP_011538284.1:p.Thr289=
XR_945791.1:n.1532_1533delinsCA
NM_000314.7:c.962_963delinsCA	NP_000305.3:p.Thr321=
NM_001304717.5:c.1481_1482delinsCA	NP_001291646.4:p.Thr494=
NM_001304718.2:c.371_372delinsCA	NP_001291647.1:p.Thr124=
NM_000314.8:c.962_963delinsCA MANE Select	NP_000305.3:p.Thr321=