Canonical Allele Identifier: CA891837751
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965387_87965388delinsCA , CM000672.2:g.87965387_87965388delinsCA GRCh38
NC_000010.10:g.89725144_89725145delinsCA , CM000672.1:g.89725144_89725145delinsCA GRCh37
NC_000010.9:g.89715124_89715125delinsCA NCBI36
NG_007466.2:g.106949_106950delinsCA , LRG_311:g.106949_106950delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1220_1221delinsCA ENSP00000514759.2:p.His407Pro
ENST00000710265.1:c.*156_*157delinsCA ENSP00000518161.1:n.*156_*157delinsCA
ENST00000688158.2:n.1862_1863delinsCA
ENST00000688922.2:c.*957_*958delinsCA ENSP00000508742.2:n.*957_*958delinsCA
ENST00000700021.1:c.1082_1083delinsCA ENSP00000514757.1:p.His361Pro
ENST00000700022.1:c.*466_*467delinsCA ENSP00000514758.1:n.*466_*467delinsCA
ENST00000700023.1:n.2285_2286delinsCA
ENST00000700024.1:n.2519_2520delinsCA
ENST00000706954.1:c.1127_1128delinsCA ENSP00000516674.1:p.His376Pro
ENST00000706955.1:c.*1162_*1163delinsCA ENSP00000516675.1:n.*1162_*1163delinsCA
ENST00000686459.1:c.*713_*714delinsCA ENSP00000508909.1:n.*713_*714delinsCA
ENST00000688158.1:c.*1238_*1239delinsCA ENSP00000509254.1:n.*1238_*1239delinsCA
ENST00000688308.1:c.1127_1128delinsCA ENSP00000508752.1:p.His376Pro
ENST00000688922.1:c.1048_1049delinsCA
ENST00000693560.1:c.1646_1647delinsCA ENSP00000509861.1:p.His549Pro
ENST00000371953.8:c.1127_1128delinsCA MANE Select ENSP00000361021.3:p.His376Pro
ENST00000371953.7:c.1127_1128delinsCA ENSP00000361021.3:p.His376Pro
NM_000314.5:c.1127_1128delinsCA NP_000305.3:p.His376Pro
NM_000314.6:c.1127_1128delinsCA NP_000305.3:p.His376Pro
NM_001304717.2:c.1646_1647delinsCA NP_001291646.2:p.His549Pro
NM_001304718.1:c.536_537delinsCA NP_001291647.1:p.His179Pro
XM_006717926.2:c.1082_1083delinsCA XP_006717989.1:p.His361Pro
XM_011539982.1:c.1031_1032delinsCA XP_011538284.1:p.His344Pro
XR_945791.1:n.1697_1698delinsCA
NM_000314.7:c.1127_1128delinsCA NP_000305.3:p.His376Pro
NM_001304717.5:c.1646_1647delinsCA NP_001291646.4:p.His549Pro
NM_001304718.2:c.536_537delinsCA NP_001291647.1:p.His179Pro
NM_000314.8:c.1127_1128delinsCA MANE Select NP_000305.3:p.His376Pro