Canonical Allele Identifier: CA2579926665

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961083_87961085del , CM000672.2:g.87961083_87961085del	GRCh38
NC_000010.10:g.89720840_89720842del , CM000672.1:g.89720840_89720842del	GRCh37
NC_000010.9:g.89710820_89710822del	NCBI36
NG_007466.2:g.102645_102647del , LRG_311:g.102645_102647del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1084_1086del	ENSP00000514759.2:p.Asp362del
ENST00000710265.1:c.991_993del	ENSP00000518161.1:p.Asp331del
ENST00000472832.3:c.991_993del	ENSP00000483066.2:p.Asp331del
ENST00000688158.2:n.1726_1728del
ENST00000688922.2:c.*821_*823del	ENSP00000508742.2:n.*821_*823del
ENST00000700021.1:c.946_948del	ENSP00000514757.1:p.Asp316del
ENST00000700022.1:c.*330_*332del	ENSP00000514758.1:n.*330_*332del
ENST00000700023.1:n.2149_2151del
ENST00000700024.1:n.2383_2385del
ENST00000700025.1:n.1760_1762del
ENST00000700026.1:n.628_630del
ENST00000706954.1:c.991_993del	ENSP00000516674.1:p.Asp331del
ENST00000706955.1:c.*1026_*1028del	ENSP00000516675.1:n.*1026_*1028del
ENST00000686459.1:c.*577_*579del	ENSP00000508909.1:n.*577_*579del
ENST00000688158.1:c.*1102_*1104del	ENSP00000509254.1:n.*1102_*1104del
ENST00000688308.1:c.991_993del	ENSP00000508752.1:p.Asp331del
ENST00000688922.1:c.912_914del
ENST00000693560.1:c.1510_1512del	ENSP00000509861.1:p.Asp504del
ENST00000371953.8:c.991_993del MANE Select	ENSP00000361021.3:p.Asp331del
ENST00000371953.7:c.991_993del	ENSP00000361021.3:p.Asp331del
ENST00000472832.2:c.418_420del	ENSP00000483066.1:p.Asp140del
NM_000314.5:c.991_993del	NP_000305.3:p.Asp331del
NM_000314.6:c.991_993del	NP_000305.3:p.Asp331del
NM_001304717.2:c.1510_1512del	NP_001291646.2:p.Asp504del
NM_001304718.1:c.400_402del	NP_001291647.1:p.Asp134del
XM_006717926.2:c.946_948del	XP_006717989.1:p.Asp316del
XM_011539981.1:c.991_993del	XP_011538283.1:p.Asp331del
XM_011539982.1:c.895_897del	XP_011538284.1:p.Asp299del
XR_945791.1:n.1561_1563del
NM_000314.7:c.991_993del	NP_000305.3:p.Asp331del
NM_001304717.5:c.1510_1512del	NP_001291646.4:p.Asp504del
NM_001304718.2:c.400_402del	NP_001291647.1:p.Asp134del
NM_000314.8:c.991_993del MANE Select	NP_000305.3:p.Asp331del