Canonical Allele Identifier: CA2579926386

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965462_87965464del , CM000672.2:g.87965462_87965464del	GRCh38
NC_000010.10:g.89725219_89725221del , CM000672.1:g.89725219_89725221del	GRCh37
NC_000010.9:g.89715199_89715201del	NCBI36
NG_007466.2:g.107024_107026del , LRG_311:g.107024_107026del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1295_1297del	ENSP00000514759.2:p.Thr432del
ENST00000710265.1:c.*231_*233del	ENSP00000518161.1:n.*231_*233del
ENST00000688158.2:n.1937_1939del
ENST00000688922.2:c.*1032_*1034del	ENSP00000508742.2:n.*1032_*1034del
ENST00000700021.1:c.1157_1159del	ENSP00000514757.1:p.Thr386del
ENST00000700022.1:c.*541_*543del	ENSP00000514758.1:n.*541_*543del
ENST00000700023.1:n.2360_2362del
ENST00000700024.1:n.2594_2596del
ENST00000706954.1:c.1202_1204del	ENSP00000516674.1:p.Thr401del
ENST00000706955.1:c.*1237_*1239del	ENSP00000516675.1:n.*1237_*1239del
ENST00000686459.1:c.*788_*790del	ENSP00000508909.1:n.*788_*790del
ENST00000688158.1:c.*1313_*1315del	ENSP00000509254.1:n.*1313_*1315del
ENST00000688308.1:c.1202_1204del	ENSP00000508752.1:p.Thr401del
ENST00000688922.1:c.1123_1125del
ENST00000693560.1:c.1721_1723del	ENSP00000509861.1:p.Thr574del
ENST00000371953.8:c.1202_1204del MANE Select	ENSP00000361021.3:p.Thr401del
ENST00000371953.7:c.1202_1204del	ENSP00000361021.3:p.Thr401del
NM_000314.5:c.1202_1204del	NP_000305.3:p.Thr401del
NM_000314.6:c.1202_1204del	NP_000305.3:p.Thr401del
NM_001304717.2:c.1721_1723del	NP_001291646.2:p.Thr574del
NM_001304718.1:c.611_613del	NP_001291647.1:p.Thr204del
XM_006717926.2:c.1157_1159del	XP_006717989.1:p.Thr386del
XM_011539982.1:c.1106_1108del	XP_011538284.1:p.Thr369del
XR_945791.1:n.1772_1774del
NM_000314.7:c.1202_1204del	NP_000305.3:p.Thr401del
NM_001304717.5:c.1721_1723del	NP_001291646.4:p.Thr574del
NM_001304718.2:c.611_613del	NP_001291647.1:p.Thr204del
NM_000314.8:c.1202_1204del MANE Select	NP_000305.3:p.Thr401del