Canonical Allele Identifier: CA891838010
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965422_87965424delinsACT , CM000672.2:g.87965422_87965424delinsACT GRCh38
NC_000010.10:g.89725179_89725181delinsACT , CM000672.1:g.89725179_89725181delinsACT GRCh37
NC_000010.9:g.89715159_89715161delinsACT NCBI36
NG_007466.2:g.106984_106986delinsACT , LRG_311:g.106984_106986delinsACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1255_1257delinsACT ENSP00000514759.2:p.Glu419Thr
ENST00000710265.1:c.*191_*193delinsACT ENSP00000518161.1:n.*191_*193delinsACT
ENST00000688158.2:n.1897_1899delinsACT
ENST00000688922.2:c.*992_*994delinsACT ENSP00000508742.2:n.*992_*994delinsACT
ENST00000700021.1:c.1117_1119delinsACT ENSP00000514757.1:p.Glu373Thr
ENST00000700022.1:c.*501_*503delinsACT ENSP00000514758.1:n.*501_*503delinsACT
ENST00000700023.1:n.2320_2322delinsACT
ENST00000700024.1:n.2554_2556delinsACT
ENST00000706954.1:c.1162_1164delinsACT ENSP00000516674.1:p.Glu388Thr
ENST00000706955.1:c.*1197_*1199delinsACT ENSP00000516675.1:n.*1197_*1199delinsACT
ENST00000686459.1:c.*748_*750delinsACT ENSP00000508909.1:n.*748_*750delinsACT
ENST00000688158.1:c.*1273_*1275delinsACT ENSP00000509254.1:n.*1273_*1275delinsACT
ENST00000688308.1:c.1162_1164delinsACT ENSP00000508752.1:p.Glu388Thr
ENST00000688922.1:c.1083_1085delinsACT
ENST00000693560.1:c.1681_1683delinsACT ENSP00000509861.1:p.Glu561Thr
ENST00000371953.8:c.1162_1164delinsACT MANE Select ENSP00000361021.3:p.Glu388Thr
ENST00000371953.7:c.1162_1164delinsACT ENSP00000361021.3:p.Glu388Thr
NM_000314.5:c.1162_1164delinsACT NP_000305.3:p.Glu388Thr
NM_000314.6:c.1162_1164delinsACT NP_000305.3:p.Glu388Thr
NM_001304717.2:c.1681_1683delinsACT NP_001291646.2:p.Glu561Thr
NM_001304718.1:c.571_573delinsACT NP_001291647.1:p.Glu191Thr
XM_006717926.2:c.1117_1119delinsACT XP_006717989.1:p.Glu373Thr
XM_011539982.1:c.1066_1068delinsACT XP_011538284.1:p.Glu356Thr
XR_945791.1:n.1732_1734delinsACT
NM_000314.7:c.1162_1164delinsACT NP_000305.3:p.Glu388Thr
NM_001304717.5:c.1681_1683delinsACT NP_001291646.4:p.Glu561Thr
NM_001304718.2:c.571_573delinsACT NP_001291647.1:p.Glu191Thr
NM_000314.8:c.1162_1164delinsACT MANE Select NP_000305.3:p.Glu388Thr