Canonical Allele Identifier: CA891838194
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965450_87965451delinsCA , CM000672.2:g.87965450_87965451delinsCA GRCh38
NC_000010.10:g.89725207_89725208delinsCA , CM000672.1:g.89725207_89725208delinsCA GRCh37
NC_000010.9:g.89715187_89715188delinsCA NCBI36
NG_007466.2:g.107012_107013delinsCA , LRG_311:g.107012_107013delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1283_1284delinsCA ENSP00000514759.2:p.His428Pro
ENST00000710265.1:c.*219_*220delinsCA ENSP00000518161.1:n.*219_*220delinsCA
ENST00000688158.2:n.1925_1926delinsCA
ENST00000688922.2:c.*1020_*1021delinsCA ENSP00000508742.2:n.*1020_*1021delinsCA
ENST00000700021.1:c.1145_1146delinsCA ENSP00000514757.1:p.His382Pro
ENST00000700022.1:c.*529_*530delinsCA ENSP00000514758.1:n.*529_*530delinsCA
ENST00000700023.1:n.2348_2349delinsCA
ENST00000700024.1:n.2582_2583delinsCA
ENST00000706954.1:c.1190_1191delinsCA ENSP00000516674.1:p.His397Pro
ENST00000706955.1:c.*1225_*1226delinsCA ENSP00000516675.1:n.*1225_*1226delinsCA
ENST00000686459.1:c.*776_*777delinsCA ENSP00000508909.1:n.*776_*777delinsCA
ENST00000688158.1:c.*1301_*1302delinsCA ENSP00000509254.1:n.*1301_*1302delinsCA
ENST00000688308.1:c.1190_1191delinsCA ENSP00000508752.1:p.His397Pro
ENST00000688922.1:c.1111_1112delinsCA
ENST00000693560.1:c.1709_1710delinsCA ENSP00000509861.1:p.His570Pro
ENST00000371953.8:c.1190_1191delinsCA MANE Select ENSP00000361021.3:p.His397Pro
ENST00000371953.7:c.1190_1191delinsCA ENSP00000361021.3:p.His397Pro
NM_000314.5:c.1190_1191delinsCA NP_000305.3:p.His397Pro
NM_000314.6:c.1190_1191delinsCA NP_000305.3:p.His397Pro
NM_001304717.2:c.1709_1710delinsCA NP_001291646.2:p.His570Pro
NM_001304718.1:c.599_600delinsCA NP_001291647.1:p.His200Pro
XM_006717926.2:c.1145_1146delinsCA XP_006717989.1:p.His382Pro
XM_011539982.1:c.1094_1095delinsCA XP_011538284.1:p.His365Pro
XR_945791.1:n.1760_1761delinsCA
NM_000314.7:c.1190_1191delinsCA NP_000305.3:p.His397Pro
NM_001304717.5:c.1709_1710delinsCA NP_001291646.4:p.His570Pro
NM_001304718.2:c.599_600delinsCA NP_001291647.1:p.His200Pro
NM_000314.8:c.1190_1191delinsCA MANE Select NP_000305.3:p.His397Pro