Canonical Allele Identifier: CA2579926404
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965422_87965424delinsATT , CM000672.2:g.87965422_87965424delinsATT GRCh38
NC_000010.10:g.89725179_89725181delinsATT , CM000672.1:g.89725179_89725181delinsATT GRCh37
NC_000010.9:g.89715159_89715161delinsATT NCBI36
NG_007466.2:g.106984_106986delinsATT , LRG_311:g.106984_106986delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1255_1257delinsATT ENSP00000514759.2:p.Glu419Ile
ENST00000710265.1:c.*191_*193delinsATT ENSP00000518161.1:n.*191_*193delinsATT
ENST00000688158.2:n.1897_1899delinsATT
ENST00000688922.2:c.*992_*994delinsATT ENSP00000508742.2:n.*992_*994delinsATT
ENST00000700021.1:c.1117_1119delinsATT ENSP00000514757.1:p.Glu373Ile
ENST00000700022.1:c.*501_*503delinsATT ENSP00000514758.1:n.*501_*503delinsATT
ENST00000700023.1:n.2320_2322delinsATT
ENST00000700024.1:n.2554_2556delinsATT
ENST00000706954.1:c.1162_1164delinsATT ENSP00000516674.1:p.Glu388Ile
ENST00000706955.1:c.*1197_*1199delinsATT ENSP00000516675.1:n.*1197_*1199delinsATT
ENST00000686459.1:c.*748_*750delinsATT ENSP00000508909.1:n.*748_*750delinsATT
ENST00000688158.1:c.*1273_*1275delinsATT ENSP00000509254.1:n.*1273_*1275delinsATT
ENST00000688308.1:c.1162_1164delinsATT ENSP00000508752.1:p.Glu388Ile
ENST00000688922.1:c.1083_1085delinsATT
ENST00000693560.1:c.1681_1683delinsATT ENSP00000509861.1:p.Glu561Ile
ENST00000371953.8:c.1162_1164delinsATT MANE Select ENSP00000361021.3:p.Glu388Ile
ENST00000371953.7:c.1162_1164delinsATT ENSP00000361021.3:p.Glu388Ile
NM_000314.5:c.1162_1164delinsATT NP_000305.3:p.Glu388Ile
NM_000314.6:c.1162_1164delinsATT NP_000305.3:p.Glu388Ile
NM_001304717.2:c.1681_1683delinsATT NP_001291646.2:p.Glu561Ile
NM_001304718.1:c.571_573delinsATT NP_001291647.1:p.Glu191Ile
XM_006717926.2:c.1117_1119delinsATT XP_006717989.1:p.Glu373Ile
XM_011539982.1:c.1066_1068delinsATT XP_011538284.1:p.Glu356Ile
XR_945791.1:n.1732_1734delinsATT
NM_000314.7:c.1162_1164delinsATT NP_000305.3:p.Glu388Ile
NM_001304717.5:c.1681_1683delinsATT NP_001291646.4:p.Glu561Ile
NM_001304718.2:c.571_573delinsATT NP_001291647.1:p.Glu191Ile
NM_000314.8:c.1162_1164delinsATT MANE Select NP_000305.3:p.Glu388Ile