Canonical Allele Identifier: CA891841724

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965461_87965463delinsTGT , CM000672.2:g.87965461_87965463delinsTGT	GRCh38
NC_000010.10:g.89725218_89725220delinsTGT , CM000672.1:g.89725218_89725220delinsTGT	GRCh37
NC_000010.9:g.89715198_89715200delinsTGT	NCBI36
NG_007466.2:g.107023_107025delinsTGT , LRG_311:g.107023_107025delinsTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1294_1296delinsTGT	ENSP00000514759.2:p.Thr432Cys
ENST00000710265.1:c.*230_*232delinsTGT	ENSP00000518161.1:n.*230_*232delinsTGT
ENST00000688158.2:n.1936_1938delinsTGT
ENST00000688922.2:c.*1031_*1033delinsTGT	ENSP00000508742.2:n.*1031_*1033delinsTGT
ENST00000700021.1:c.1156_1158delinsTGT	ENSP00000514757.1:p.Thr386Cys
ENST00000700022.1:c.*540_*542delinsTGT	ENSP00000514758.1:n.*540_*542delinsTGT
ENST00000700023.1:n.2359_2361delinsTGT
ENST00000700024.1:n.2593_2595delinsTGT
ENST00000706954.1:c.1201_1203delinsTGT	ENSP00000516674.1:p.Thr401Cys
ENST00000706955.1:c.*1236_*1238delinsTGT	ENSP00000516675.1:n.*1236_*1238delinsTGT
ENST00000686459.1:c.*787_*789delinsTGT	ENSP00000508909.1:n.*787_*789delinsTGT
ENST00000688158.1:c.*1312_*1314delinsTGT	ENSP00000509254.1:n.*1312_*1314delinsTGT
ENST00000688308.1:c.1201_1203delinsTGT	ENSP00000508752.1:p.Thr401Cys
ENST00000688922.1:c.1122_1124delinsTGT
ENST00000693560.1:c.1720_1722delinsTGT	ENSP00000509861.1:p.Thr574Cys
ENST00000371953.8:c.1201_1203delinsTGT MANE Select	ENSP00000361021.3:p.Thr401Cys
ENST00000371953.7:c.1201_1203delinsTGT	ENSP00000361021.3:p.Thr401Cys
NM_000314.5:c.1201_1203delinsTGT	NP_000305.3:p.Thr401Cys
NM_000314.6:c.1201_1203delinsTGT	NP_000305.3:p.Thr401Cys
NM_001304717.2:c.1720_1722delinsTGT	NP_001291646.2:p.Thr574Cys
NM_001304718.1:c.610_612delinsTGT	NP_001291647.1:p.Thr204Cys
XM_006717926.2:c.1156_1158delinsTGT	XP_006717989.1:p.Thr386Cys
XM_011539982.1:c.1105_1107delinsTGT	XP_011538284.1:p.Thr369Cys
XR_945791.1:n.1771_1773delinsTGT
NM_000314.7:c.1201_1203delinsTGT	NP_000305.3:p.Thr401Cys
NM_001304717.5:c.1720_1722delinsTGT	NP_001291646.4:p.Thr574Cys
NM_001304718.2:c.610_612delinsTGT	NP_001291647.1:p.Thr204Cys
NM_000314.8:c.1201_1203delinsTGT MANE Select	NP_000305.3:p.Thr401Cys