Canonical Allele Identifier: CA891840849
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957978_87957979delinsGT , CM000672.2:g.87957978_87957979delinsGT GRCh38
NC_000010.10:g.89717735_89717736delinsGT , CM000672.1:g.89717735_89717736delinsGT GRCh37
NC_000010.9:g.89707715_89707716delinsGT NCBI36
NG_007466.2:g.99540_99541delinsGT , LRG_311:g.99540_99541delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.760_761delinsGT ENSP00000514759.2:p.Lys254Val
ENST00000710265.1:c.760_761delinsGT ENSP00000518161.1:p.Lys254Val
ENST00000472832.3:c.760_761delinsGT ENSP00000483066.2:p.Lys254Val
ENST00000688158.2:n.1495_1496delinsGT
ENST00000688922.2:c.*590_*591delinsGT ENSP00000508742.2:n.*590_*591delinsGT
ENST00000700021.1:c.715_716delinsGT ENSP00000514757.1:p.Lys239Val
ENST00000700022.1:c.*99_*100delinsGT ENSP00000514758.1:n.*99_*100delinsGT
ENST00000700023.1:n.1918_1919delinsGT
ENST00000700024.1:n.2152_2153delinsGT
ENST00000700025.1:n.1529_1530delinsGT
ENST00000700026.1:n.397_398delinsGT
ENST00000700029.1:c.594_595delinsGT
ENST00000706954.1:c.760_761delinsGT ENSP00000516674.1:p.Lys254Val
ENST00000706955.1:c.*795_*796delinsGT ENSP00000516675.1:n.*795_*796delinsGT
ENST00000686459.1:c.*346_*347delinsGT ENSP00000508909.1:n.*346_*347delinsGT
ENST00000688158.1:c.*871_*872delinsGT ENSP00000509254.1:n.*871_*872delinsGT
ENST00000688308.1:c.760_761delinsGT ENSP00000508752.1:p.Lys254Val
ENST00000688922.1:c.681_682delinsGT
ENST00000693560.1:c.1279_1280delinsGT ENSP00000509861.1:p.Lys427Val
ENST00000371953.8:c.760_761delinsGT MANE Select ENSP00000361021.3:p.Lys254Val
ENST00000371953.7:c.760_761delinsGT ENSP00000361021.3:p.Lys254Val
ENST00000472832.2:c.187_188delinsGT ENSP00000483066.1:p.Lys63Val
NM_000314.5:c.760_761delinsGT NP_000305.3:p.Lys254Val
NM_000314.6:c.760_761delinsGT NP_000305.3:p.Lys254Val
NM_001304717.2:c.1279_1280delinsGT NP_001291646.2:p.Lys427Val
NM_001304718.1:c.169_170delinsGT NP_001291647.1:p.Lys57Val
XM_006717926.2:c.715_716delinsGT XP_006717989.1:p.Lys239Val
XM_011539981.1:c.760_761delinsGT XP_011538283.1:p.Lys254Val
XM_011539982.1:c.664_665delinsGT XP_011538284.1:p.Lys222Val
XR_945791.1:n.1330_1331delinsGT
NM_000314.7:c.760_761delinsGT NP_000305.3:p.Lys254Val
NM_001304717.5:c.1279_1280delinsGT NP_001291646.4:p.Lys427Val
NM_001304718.2:c.169_170delinsGT NP_001291647.1:p.Lys57Val
NM_000314.8:c.760_761delinsGT MANE Select NP_000305.3:p.Lys254Val