Canonical Allele Identifier: CA891837943
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965411_87965412delinsCT , CM000672.2:g.87965411_87965412delinsCT GRCh38
NC_000010.10:g.89725168_89725169delinsCT , CM000672.1:g.89725168_89725169delinsCT GRCh37
NC_000010.9:g.89715148_89715149delinsCT NCBI36
NG_007466.2:g.106973_106974delinsCT , LRG_311:g.106973_106974delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1244_1245delinsCT ENSP00000514759.2:p.Asp415Ala
ENST00000710265.1:c.*180_*181delinsCT ENSP00000518161.1:n.*180_*181delinsCT
ENST00000688158.2:n.1886_1887delinsCT
ENST00000688922.2:c.*981_*982delinsCT ENSP00000508742.2:n.*981_*982delinsCT
ENST00000700021.1:c.1106_1107delinsCT ENSP00000514757.1:p.Asp369Ala
ENST00000700022.1:c.*490_*491delinsCT ENSP00000514758.1:n.*490_*491delinsCT
ENST00000700023.1:n.2309_2310delinsCT
ENST00000700024.1:n.2543_2544delinsCT
ENST00000706954.1:c.1151_1152delinsCT ENSP00000516674.1:p.Asp384Ala
ENST00000706955.1:c.*1186_*1187delinsCT ENSP00000516675.1:n.*1186_*1187delinsCT
ENST00000686459.1:c.*737_*738delinsCT ENSP00000508909.1:n.*737_*738delinsCT
ENST00000688158.1:c.*1262_*1263delinsCT ENSP00000509254.1:n.*1262_*1263delinsCT
ENST00000688308.1:c.1151_1152delinsCT ENSP00000508752.1:p.Asp384Ala
ENST00000688922.1:c.1072_1073delinsCT
ENST00000693560.1:c.1670_1671delinsCT ENSP00000509861.1:p.Asp557Ala
ENST00000371953.8:c.1151_1152delinsCT MANE Select ENSP00000361021.3:p.Asp384Ala
ENST00000371953.7:c.1151_1152delinsCT ENSP00000361021.3:p.Asp384Ala
NM_000314.5:c.1151_1152delinsCT NP_000305.3:p.Asp384Ala
NM_000314.6:c.1151_1152delinsCT NP_000305.3:p.Asp384Ala
NM_001304717.2:c.1670_1671delinsCT NP_001291646.2:p.Asp557Ala
NM_001304718.1:c.560_561delinsCT NP_001291647.1:p.Asp187Ala
XM_006717926.2:c.1106_1107delinsCT XP_006717989.1:p.Asp369Ala
XM_011539982.1:c.1055_1056delinsCT XP_011538284.1:p.Asp352Ala
XR_945791.1:n.1721_1722delinsCT
NM_000314.7:c.1151_1152delinsCT NP_000305.3:p.Asp384Ala
NM_001304717.5:c.1670_1671delinsCT NP_001291646.4:p.Asp557Ala
NM_001304718.2:c.560_561delinsCT NP_001291647.1:p.Asp187Ala
NM_000314.8:c.1151_1152delinsCT MANE Select NP_000305.3:p.Asp384Ala