Canonical Allele Identifier: CA891839936
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957978_87957980delinsTAT , CM000672.2:g.87957978_87957980delinsTAT GRCh38
NC_000010.10:g.89717735_89717737delinsTAT , CM000672.1:g.89717735_89717737delinsTAT GRCh37
NC_000010.9:g.89707715_89707717delinsTAT NCBI36
NG_007466.2:g.99540_99542delinsTAT , LRG_311:g.99540_99542delinsTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.760_762delinsTAT ENSP00000514759.2:p.Lys254Tyr
ENST00000710265.1:c.760_762delinsTAT ENSP00000518161.1:p.Lys254Tyr
ENST00000472832.3:c.760_762delinsTAT ENSP00000483066.2:p.Lys254Tyr
ENST00000688158.2:n.1495_1497delinsTAT
ENST00000688922.2:c.*590_*592delinsTAT ENSP00000508742.2:n.*590_*592delinsTAT
ENST00000700021.1:c.715_717delinsTAT ENSP00000514757.1:p.Lys239Tyr
ENST00000700022.1:c.*99_*101delinsTAT ENSP00000514758.1:n.*99_*101delinsTAT
ENST00000700023.1:n.1918_1920delinsTAT
ENST00000700024.1:n.2152_2154delinsTAT
ENST00000700025.1:n.1529_1531delinsTAT
ENST00000700026.1:n.397_399delinsTAT
ENST00000700029.1:c.594_596delinsTAT
ENST00000706954.1:c.760_762delinsTAT ENSP00000516674.1:p.Lys254Tyr
ENST00000706955.1:c.*795_*797delinsTAT ENSP00000516675.1:n.*795_*797delinsTAT
ENST00000686459.1:c.*346_*348delinsTAT ENSP00000508909.1:n.*346_*348delinsTAT
ENST00000688158.1:c.*871_*873delinsTAT ENSP00000509254.1:n.*871_*873delinsTAT
ENST00000688308.1:c.760_762delinsTAT ENSP00000508752.1:p.Lys254Tyr
ENST00000688922.1:c.681_683delinsTAT
ENST00000693560.1:c.1279_1281delinsTAT ENSP00000509861.1:p.Lys427Tyr
ENST00000371953.8:c.760_762delinsTAT MANE Select ENSP00000361021.3:p.Lys254Tyr
ENST00000371953.7:c.760_762delinsTAT ENSP00000361021.3:p.Lys254Tyr
ENST00000472832.2:c.187_189delinsTAT ENSP00000483066.1:p.Lys63Tyr
NM_000314.5:c.760_762delinsTAT NP_000305.3:p.Lys254Tyr
NM_000314.6:c.760_762delinsTAT NP_000305.3:p.Lys254Tyr
NM_001304717.2:c.1279_1281delinsTAT NP_001291646.2:p.Lys427Tyr
NM_001304718.1:c.169_171delinsTAT NP_001291647.1:p.Lys57Tyr
XM_006717926.2:c.715_717delinsTAT XP_006717989.1:p.Lys239Tyr
XM_011539981.1:c.760_762delinsTAT XP_011538283.1:p.Lys254Tyr
XM_011539982.1:c.664_666delinsTAT XP_011538284.1:p.Lys222Tyr
XR_945791.1:n.1330_1332delinsTAT
NM_000314.7:c.760_762delinsTAT NP_000305.3:p.Lys254Tyr
NM_001304717.5:c.1279_1281delinsTAT NP_001291646.4:p.Lys427Tyr
NM_001304718.2:c.169_171delinsTAT NP_001291647.1:p.Lys57Tyr
NM_000314.8:c.760_762delinsTAT MANE Select NP_000305.3:p.Lys254Tyr