Canonical Allele Identifier: CA891837139

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965320_87965322delinsGAT , CM000672.2:g.87965320_87965322delinsGAT	GRCh38
NC_000010.10:g.89725077_89725079delinsGAT , CM000672.1:g.89725077_89725079delinsGAT	GRCh37
NC_000010.9:g.89715057_89715059delinsGAT	NCBI36
NG_007466.2:g.106882_106884delinsGAT , LRG_311:g.106882_106884delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1153_1155delinsGAT	ENSP00000514759.2:p.Pro385Asp
ENST00000710265.1:c.*89_*91delinsGAT	ENSP00000518161.1:n.*89_*91delinsGAT
ENST00000688158.2:n.1795_1797delinsGAT
ENST00000688922.2:c.*890_*892delinsGAT	ENSP00000508742.2:n.*890_*892delinsGAT
ENST00000700021.1:c.1015_1017delinsGAT	ENSP00000514757.1:p.Pro339Asp
ENST00000700022.1:c.*399_*401delinsGAT	ENSP00000514758.1:n.*399_*401delinsGAT
ENST00000700023.1:n.2218_2220delinsGAT
ENST00000700024.1:n.2452_2454delinsGAT
ENST00000706954.1:c.1060_1062delinsGAT	ENSP00000516674.1:p.Pro354Asp
ENST00000706955.1:c.*1095_*1097delinsGAT	ENSP00000516675.1:n.*1095_*1097delinsGAT
ENST00000686459.1:c.*646_*648delinsGAT	ENSP00000508909.1:n.*646_*648delinsGAT
ENST00000688158.1:c.*1171_*1173delinsGAT	ENSP00000509254.1:n.*1171_*1173delinsGAT
ENST00000688308.1:c.1060_1062delinsGAT	ENSP00000508752.1:p.Pro354Asp
ENST00000688922.1:c.981_983delinsGAT
ENST00000693560.1:c.1579_1581delinsGAT	ENSP00000509861.1:p.Pro527Asp
ENST00000371953.8:c.1060_1062delinsGAT MANE Select	ENSP00000361021.3:p.Pro354Asp
ENST00000371953.7:c.1060_1062delinsGAT	ENSP00000361021.3:p.Pro354Asp
NM_000314.5:c.1060_1062delinsGAT	NP_000305.3:p.Pro354Asp
NM_000314.6:c.1060_1062delinsGAT	NP_000305.3:p.Pro354Asp
NM_001304717.2:c.1579_1581delinsGAT	NP_001291646.2:p.Pro527Asp
NM_001304718.1:c.469_471delinsGAT	NP_001291647.1:p.Pro157Asp
XM_006717926.2:c.1015_1017delinsGAT	XP_006717989.1:p.Pro339Asp
XM_011539982.1:c.964_966delinsGAT	XP_011538284.1:p.Pro322Asp
XR_945791.1:n.1630_1632delinsGAT
NM_000314.7:c.1060_1062delinsGAT	NP_000305.3:p.Pro354Asp
NM_001304717.5:c.1579_1581delinsGAT	NP_001291646.4:p.Pro527Asp
NM_001304718.2:c.469_471delinsGAT	NP_001291647.1:p.Pro157Asp
NM_000314.8:c.1060_1062delinsGAT MANE Select	NP_000305.3:p.Pro354Asp