Canonical Allele Identifier: CA2579926451

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965338_87965340delinsTCT , CM000672.2:g.87965338_87965340delinsTCT	GRCh38
NC_000010.10:g.89725095_89725097delinsTCT , CM000672.1:g.89725095_89725097delinsTCT	GRCh37
NC_000010.9:g.89715075_89715077delinsTCT	NCBI36
NG_007466.2:g.106900_106902delinsTCT , LRG_311:g.106900_106902delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1171_1173delinsTCT	ENSP00000514759.2:p.Ser391=
ENST00000710265.1:c.*107_*109delinsTCT	ENSP00000518161.1:n.*107_*109delinsTCT
ENST00000688158.2:n.1813_1815delinsTCT
ENST00000688922.2:c.*908_*910delinsTCT	ENSP00000508742.2:n.*908_*910delinsTCT
ENST00000700021.1:c.1033_1035delinsTCT	ENSP00000514757.1:p.Ser345=
ENST00000700022.1:c.*417_*419delinsTCT	ENSP00000514758.1:n.*417_*419delinsTCT
ENST00000700023.1:n.2236_2238delinsTCT
ENST00000700024.1:n.2470_2472delinsTCT
ENST00000706954.1:c.1078_1080delinsTCT	ENSP00000516674.1:p.Ser360=
ENST00000706955.1:c.*1113_*1115delinsTCT	ENSP00000516675.1:n.*1113_*1115delinsTCT
ENST00000686459.1:c.*664_*666delinsTCT	ENSP00000508909.1:n.*664_*666delinsTCT
ENST00000688158.1:c.*1189_*1191delinsTCT	ENSP00000509254.1:n.*1189_*1191delinsTCT
ENST00000688308.1:c.1078_1080delinsTCT	ENSP00000508752.1:p.Ser360=
ENST00000688922.1:c.999_1001delinsTCT
ENST00000693560.1:c.1597_1599delinsTCT	ENSP00000509861.1:p.Ser533=
ENST00000371953.8:c.1078_1080delinsTCT MANE Select	ENSP00000361021.3:p.Ser360=
ENST00000371953.7:c.1078_1080delinsTCT	ENSP00000361021.3:p.Ser360=
NM_000314.5:c.1078_1080delinsTCT	NP_000305.3:p.Ser360=
NM_000314.6:c.1078_1080delinsTCT	NP_000305.3:p.Ser360=
NM_001304717.2:c.1597_1599delinsTCT	NP_001291646.2:p.Ser533=
NM_001304718.1:c.487_489delinsTCT	NP_001291647.1:p.Ser163=
XM_006717926.2:c.1033_1035delinsTCT	XP_006717989.1:p.Ser345=
XM_011539982.1:c.982_984delinsTCT	XP_011538284.1:p.Ser328=
XR_945791.1:n.1648_1650delinsTCT
NM_000314.7:c.1078_1080delinsTCT	NP_000305.3:p.Ser360=
NM_001304717.5:c.1597_1599delinsTCT	NP_001291646.4:p.Ser533=
NM_001304718.2:c.487_489delinsTCT	NP_001291647.1:p.Ser163=
NM_000314.8:c.1078_1080delinsTCT MANE Select	NP_000305.3:p.Ser360=