Canonical Allele Identifier: CA891837276

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965333_87965334delinsTT , CM000672.2:g.87965333_87965334delinsTT	GRCh38
NC_000010.10:g.89725090_89725091delinsTT , CM000672.1:g.89725090_89725091delinsTT	GRCh37
NC_000010.9:g.89715070_89715071delinsTT	NCBI36
NG_007466.2:g.106895_106896delinsTT , LRG_311:g.106895_106896delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1166_1167delinsTT	ENSP00000514759.2:p.Glu389Val
ENST00000710265.1:c.*102_*103delinsTT	ENSP00000518161.1:n.*102_*103delinsTT
ENST00000688158.2:n.1808_1809delinsTT
ENST00000688922.2:c.*903_*904delinsTT	ENSP00000508742.2:n.*903_*904delinsTT
ENST00000700021.1:c.1028_1029delinsTT	ENSP00000514757.1:p.Glu343Val
ENST00000700022.1:c.*412_*413delinsTT	ENSP00000514758.1:n.*412_*413delinsTT
ENST00000700023.1:n.2231_2232delinsTT
ENST00000700024.1:n.2465_2466delinsTT
ENST00000706954.1:c.1073_1074delinsTT	ENSP00000516674.1:p.Glu358Val
ENST00000706955.1:c.*1108_*1109delinsTT	ENSP00000516675.1:n.*1108_*1109delinsTT
ENST00000686459.1:c.*659_*660delinsTT	ENSP00000508909.1:n.*659_*660delinsTT
ENST00000688158.1:c.*1184_*1185delinsTT	ENSP00000509254.1:n.*1184_*1185delinsTT
ENST00000688308.1:c.1073_1074delinsTT	ENSP00000508752.1:p.Glu358Val
ENST00000688922.1:c.994_995delinsTT
ENST00000693560.1:c.1592_1593delinsTT	ENSP00000509861.1:p.Glu531Val
ENST00000371953.8:c.1073_1074delinsTT MANE Select	ENSP00000361021.3:p.Glu358Val
ENST00000371953.7:c.1073_1074delinsTT	ENSP00000361021.3:p.Glu358Val
NM_000314.5:c.1073_1074delinsTT	NP_000305.3:p.Glu358Val
NM_000314.6:c.1073_1074delinsTT	NP_000305.3:p.Glu358Val
NM_001304717.2:c.1592_1593delinsTT	NP_001291646.2:p.Glu531Val
NM_001304718.1:c.482_483delinsTT	NP_001291647.1:p.Glu161Val
XM_006717926.2:c.1028_1029delinsTT	XP_006717989.1:p.Glu343Val
XM_011539982.1:c.977_978delinsTT	XP_011538284.1:p.Glu326Val
XR_945791.1:n.1643_1644delinsTT
NM_000314.7:c.1073_1074delinsTT	NP_000305.3:p.Glu358Val
NM_001304717.5:c.1592_1593delinsTT	NP_001291646.4:p.Glu531Val
NM_001304718.2:c.482_483delinsTT	NP_001291647.1:p.Glu161Val
NM_000314.8:c.1073_1074delinsTT MANE Select	NP_000305.3:p.Glu358Val