Canonical Allele Identifier: CA891840848
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957978_87957979delinsTT , CM000672.2:g.87957978_87957979delinsTT GRCh38
NC_000010.10:g.89717735_89717736delinsTT , CM000672.1:g.89717735_89717736delinsTT GRCh37
NC_000010.9:g.89707715_89707716delinsTT NCBI36
NG_007466.2:g.99540_99541delinsTT , LRG_311:g.99540_99541delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.760_761delinsTT ENSP00000514759.2:p.Lys254Leu
ENST00000710265.1:c.760_761delinsTT ENSP00000518161.1:p.Lys254Leu
ENST00000472832.3:c.760_761delinsTT ENSP00000483066.2:p.Lys254Leu
ENST00000688158.2:n.1495_1496delinsTT
ENST00000688922.2:c.*590_*591delinsTT ENSP00000508742.2:n.*590_*591delinsTT
ENST00000700021.1:c.715_716delinsTT ENSP00000514757.1:p.Lys239Leu
ENST00000700022.1:c.*99_*100delinsTT ENSP00000514758.1:n.*99_*100delinsTT
ENST00000700023.1:n.1918_1919delinsTT
ENST00000700024.1:n.2152_2153delinsTT
ENST00000700025.1:n.1529_1530delinsTT
ENST00000700026.1:n.397_398delinsTT
ENST00000700029.1:c.594_595delinsTT
ENST00000706954.1:c.760_761delinsTT ENSP00000516674.1:p.Lys254Leu
ENST00000706955.1:c.*795_*796delinsTT ENSP00000516675.1:n.*795_*796delinsTT
ENST00000686459.1:c.*346_*347delinsTT ENSP00000508909.1:n.*346_*347delinsTT
ENST00000688158.1:c.*871_*872delinsTT ENSP00000509254.1:n.*871_*872delinsTT
ENST00000688308.1:c.760_761delinsTT ENSP00000508752.1:p.Lys254Leu
ENST00000688922.1:c.681_682delinsTT
ENST00000693560.1:c.1279_1280delinsTT ENSP00000509861.1:p.Lys427Leu
ENST00000371953.8:c.760_761delinsTT MANE Select ENSP00000361021.3:p.Lys254Leu
ENST00000371953.7:c.760_761delinsTT ENSP00000361021.3:p.Lys254Leu
ENST00000472832.2:c.187_188delinsTT ENSP00000483066.1:p.Lys63Leu
NM_000314.5:c.760_761delinsTT NP_000305.3:p.Lys254Leu
NM_000314.6:c.760_761delinsTT NP_000305.3:p.Lys254Leu
NM_001304717.2:c.1279_1280delinsTT NP_001291646.2:p.Lys427Leu
NM_001304718.1:c.169_170delinsTT NP_001291647.1:p.Lys57Leu
XM_006717926.2:c.715_716delinsTT XP_006717989.1:p.Lys239Leu
XM_011539981.1:c.760_761delinsTT XP_011538283.1:p.Lys254Leu
XM_011539982.1:c.664_665delinsTT XP_011538284.1:p.Lys222Leu
XR_945791.1:n.1330_1331delinsTT
NM_000314.7:c.760_761delinsTT NP_000305.3:p.Lys254Leu
NM_001304717.5:c.1279_1280delinsTT NP_001291646.4:p.Lys427Leu
NM_001304718.2:c.169_170delinsTT NP_001291647.1:p.Lys57Leu
NM_000314.8:c.760_761delinsTT MANE Select NP_000305.3:p.Lys254Leu