Canonical Allele Identifier: CA891841719

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965461_87965462delinsGT , CM000672.2:g.87965461_87965462delinsGT	GRCh38
NC_000010.10:g.89725218_89725219delinsGT , CM000672.1:g.89725218_89725219delinsGT	GRCh37
NC_000010.9:g.89715198_89715199delinsGT	NCBI36
NG_007466.2:g.107023_107024delinsGT , LRG_311:g.107023_107024delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1294_1295delinsGT	ENSP00000514759.2:p.Thr432Val
ENST00000710265.1:c.*230_*231delinsGT	ENSP00000518161.1:n.*230_*231delinsGT
ENST00000688158.2:n.1936_1937delinsGT
ENST00000688922.2:c.*1031_*1032delinsGT	ENSP00000508742.2:n.*1031_*1032delinsGT
ENST00000700021.1:c.1156_1157delinsGT	ENSP00000514757.1:p.Thr386Val
ENST00000700022.1:c.*540_*541delinsGT	ENSP00000514758.1:n.*540_*541delinsGT
ENST00000700023.1:n.2359_2360delinsGT
ENST00000700024.1:n.2593_2594delinsGT
ENST00000706954.1:c.1201_1202delinsGT	ENSP00000516674.1:p.Thr401Val
ENST00000706955.1:c.*1236_*1237delinsGT	ENSP00000516675.1:n.*1236_*1237delinsGT
ENST00000686459.1:c.*787_*788delinsGT	ENSP00000508909.1:n.*787_*788delinsGT
ENST00000688158.1:c.*1312_*1313delinsGT	ENSP00000509254.1:n.*1312_*1313delinsGT
ENST00000688308.1:c.1201_1202delinsGT	ENSP00000508752.1:p.Thr401Val
ENST00000688922.1:c.1122_1123delinsGT
ENST00000693560.1:c.1720_1721delinsGT	ENSP00000509861.1:p.Thr574Val
ENST00000371953.8:c.1201_1202delinsGT MANE Select	ENSP00000361021.3:p.Thr401Val
ENST00000371953.7:c.1201_1202delinsGT	ENSP00000361021.3:p.Thr401Val
NM_000314.5:c.1201_1202delinsGT	NP_000305.3:p.Thr401Val
NM_000314.6:c.1201_1202delinsGT	NP_000305.3:p.Thr401Val
NM_001304717.2:c.1720_1721delinsGT	NP_001291646.2:p.Thr574Val
NM_001304718.1:c.610_611delinsGT	NP_001291647.1:p.Thr204Val
XM_006717926.2:c.1156_1157delinsGT	XP_006717989.1:p.Thr386Val
XM_011539982.1:c.1105_1106delinsGT	XP_011538284.1:p.Thr369Val
XR_945791.1:n.1771_1772delinsGT
NM_000314.7:c.1201_1202delinsGT	NP_000305.3:p.Thr401Val
NM_001304717.5:c.1720_1721delinsGT	NP_001291646.4:p.Thr574Val
NM_001304718.2:c.610_611delinsGT	NP_001291647.1:p.Thr204Val
NM_000314.8:c.1201_1202delinsGT MANE Select	NP_000305.3:p.Thr401Val