Canonical Allele Identifier: CA891837151

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965320_87965322delinsATT , CM000672.2:g.87965320_87965322delinsATT	GRCh38
NC_000010.10:g.89725077_89725079delinsATT , CM000672.1:g.89725077_89725079delinsATT	GRCh37
NC_000010.9:g.89715057_89715059delinsATT	NCBI36
NG_007466.2:g.106882_106884delinsATT , LRG_311:g.106882_106884delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1153_1155delinsATT	ENSP00000514759.2:p.Pro385Ile
ENST00000710265.1:c.*89_*91delinsATT	ENSP00000518161.1:n.*89_*91delinsATT
ENST00000688158.2:n.1795_1797delinsATT
ENST00000688922.2:c.*890_*892delinsATT	ENSP00000508742.2:n.*890_*892delinsATT
ENST00000700021.1:c.1015_1017delinsATT	ENSP00000514757.1:p.Pro339Ile
ENST00000700022.1:c.*399_*401delinsATT	ENSP00000514758.1:n.*399_*401delinsATT
ENST00000700023.1:n.2218_2220delinsATT
ENST00000700024.1:n.2452_2454delinsATT
ENST00000706954.1:c.1060_1062delinsATT	ENSP00000516674.1:p.Pro354Ile
ENST00000706955.1:c.*1095_*1097delinsATT	ENSP00000516675.1:n.*1095_*1097delinsATT
ENST00000686459.1:c.*646_*648delinsATT	ENSP00000508909.1:n.*646_*648delinsATT
ENST00000688158.1:c.*1171_*1173delinsATT	ENSP00000509254.1:n.*1171_*1173delinsATT
ENST00000688308.1:c.1060_1062delinsATT	ENSP00000508752.1:p.Pro354Ile
ENST00000688922.1:c.981_983delinsATT
ENST00000693560.1:c.1579_1581delinsATT	ENSP00000509861.1:p.Pro527Ile
ENST00000371953.8:c.1060_1062delinsATT MANE Select	ENSP00000361021.3:p.Pro354Ile
ENST00000371953.7:c.1060_1062delinsATT	ENSP00000361021.3:p.Pro354Ile
NM_000314.5:c.1060_1062delinsATT	NP_000305.3:p.Pro354Ile
NM_000314.6:c.1060_1062delinsATT	NP_000305.3:p.Pro354Ile
NM_001304717.2:c.1579_1581delinsATT	NP_001291646.2:p.Pro527Ile
NM_001304718.1:c.469_471delinsATT	NP_001291647.1:p.Pro157Ile
XM_006717926.2:c.1015_1017delinsATT	XP_006717989.1:p.Pro339Ile
XM_011539982.1:c.964_966delinsATT	XP_011538284.1:p.Pro322Ile
XR_945791.1:n.1630_1632delinsATT
NM_000314.7:c.1060_1062delinsATT	NP_000305.3:p.Pro354Ile
NM_001304717.5:c.1579_1581delinsATT	NP_001291646.4:p.Pro527Ile
NM_001304718.2:c.469_471delinsATT	NP_001291647.1:p.Pro157Ile
NM_000314.8:c.1060_1062delinsATT MANE Select	NP_000305.3:p.Pro354Ile