Canonical Allele Identifier: CA891840021
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957994_87957995delinsCA , CM000672.2:g.87957994_87957995delinsCA GRCh38
NC_000010.10:g.89717751_89717752delinsCA , CM000672.1:g.89717751_89717752delinsCA GRCh37
NC_000010.9:g.89707731_89707732delinsCA NCBI36
NG_007466.2:g.99556_99557delinsCA , LRG_311:g.99556_99557delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.776_777delinsCA ENSP00000514759.2:p.His259Pro
ENST00000710265.1:c.776_777delinsCA ENSP00000518161.1:p.His259Pro
ENST00000472832.3:c.776_777delinsCA ENSP00000483066.2:p.His259Pro
ENST00000688158.2:n.1511_1512delinsCA
ENST00000688922.2:c.*606_*607delinsCA ENSP00000508742.2:n.*606_*607delinsCA
ENST00000700021.1:c.731_732delinsCA ENSP00000514757.1:p.His244Pro
ENST00000700022.1:c.*115_*116delinsCA ENSP00000514758.1:n.*115_*116delinsCA
ENST00000700023.1:n.1934_1935delinsCA
ENST00000700024.1:n.2168_2169delinsCA
ENST00000700025.1:n.1545_1546delinsCA
ENST00000700026.1:n.413_414delinsCA
ENST00000700029.1:c.610_611delinsCA
ENST00000706954.1:c.776_777delinsCA ENSP00000516674.1:p.His259Pro
ENST00000706955.1:c.*811_*812delinsCA ENSP00000516675.1:n.*811_*812delinsCA
ENST00000686459.1:c.*362_*363delinsCA ENSP00000508909.1:n.*362_*363delinsCA
ENST00000688158.1:c.*887_*888delinsCA ENSP00000509254.1:n.*887_*888delinsCA
ENST00000688308.1:c.776_777delinsCA ENSP00000508752.1:p.His259Pro
ENST00000688922.1:c.697_698delinsCA
ENST00000693560.1:c.1295_1296delinsCA ENSP00000509861.1:p.His432Pro
ENST00000371953.8:c.776_777delinsCA MANE Select ENSP00000361021.3:p.His259Pro
ENST00000371953.7:c.776_777delinsCA ENSP00000361021.3:p.His259Pro
ENST00000472832.2:c.203_204delinsCA ENSP00000483066.1:p.His68Pro
NM_000314.5:c.776_777delinsCA NP_000305.3:p.His259Pro
NM_000314.6:c.776_777delinsCA NP_000305.3:p.His259Pro
NM_001304717.2:c.1295_1296delinsCA NP_001291646.2:p.His432Pro
NM_001304718.1:c.185_186delinsCA NP_001291647.1:p.His62Pro
XM_006717926.2:c.731_732delinsCA XP_006717989.1:p.His244Pro
XM_011539981.1:c.776_777delinsCA XP_011538283.1:p.His259Pro
XM_011539982.1:c.680_681delinsCA XP_011538284.1:p.His227Pro
XR_945791.1:n.1346_1347delinsCA
NM_000314.7:c.776_777delinsCA NP_000305.3:p.His259Pro
NM_001304717.5:c.1295_1296delinsCA NP_001291646.4:p.His432Pro
NM_001304718.2:c.185_186delinsCA NP_001291647.1:p.His62Pro
NM_000314.8:c.776_777delinsCA MANE Select NP_000305.3:p.His259Pro