Canonical Allele Identifier: CA891841657
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965422_87965423delinsAT , CM000672.2:g.87965422_87965423delinsAT GRCh38
NC_000010.10:g.89725179_89725180delinsAT , CM000672.1:g.89725179_89725180delinsAT GRCh37
NC_000010.9:g.89715159_89715160delinsAT NCBI36
NG_007466.2:g.106984_106985delinsAT , LRG_311:g.106984_106985delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1255_1256delinsAT ENSP00000514759.2:p.Glu419Met
ENST00000710265.1:c.*191_*192delinsAT ENSP00000518161.1:n.*191_*192delinsAT
ENST00000688158.2:n.1897_1898delinsAT
ENST00000688922.2:c.*992_*993delinsAT ENSP00000508742.2:n.*992_*993delinsAT
ENST00000700021.1:c.1117_1118delinsAT ENSP00000514757.1:p.Glu373Met
ENST00000700022.1:c.*501_*502delinsAT ENSP00000514758.1:n.*501_*502delinsAT
ENST00000700023.1:n.2320_2321delinsAT
ENST00000700024.1:n.2554_2555delinsAT
ENST00000706954.1:c.1162_1163delinsAT ENSP00000516674.1:p.Glu388Met
ENST00000706955.1:c.*1197_*1198delinsAT ENSP00000516675.1:n.*1197_*1198delinsAT
ENST00000686459.1:c.*748_*749delinsAT ENSP00000508909.1:n.*748_*749delinsAT
ENST00000688158.1:c.*1273_*1274delinsAT ENSP00000509254.1:n.*1273_*1274delinsAT
ENST00000688308.1:c.1162_1163delinsAT ENSP00000508752.1:p.Glu388Met
ENST00000688922.1:c.1083_1084delinsAT
ENST00000693560.1:c.1681_1682delinsAT ENSP00000509861.1:p.Glu561Met
ENST00000371953.8:c.1162_1163delinsAT MANE Select ENSP00000361021.3:p.Glu388Met
ENST00000371953.7:c.1162_1163delinsAT ENSP00000361021.3:p.Glu388Met
NM_000314.5:c.1162_1163delinsAT NP_000305.3:p.Glu388Met
NM_000314.6:c.1162_1163delinsAT NP_000305.3:p.Glu388Met
NM_001304717.2:c.1681_1682delinsAT NP_001291646.2:p.Glu561Met
NM_001304718.1:c.571_572delinsAT NP_001291647.1:p.Glu191Met
XM_006717926.2:c.1117_1118delinsAT XP_006717989.1:p.Glu373Met
XM_011539982.1:c.1066_1067delinsAT XP_011538284.1:p.Glu356Met
XR_945791.1:n.1732_1733delinsAT
NM_000314.7:c.1162_1163delinsAT NP_000305.3:p.Glu388Met
NM_001304717.5:c.1681_1682delinsAT NP_001291646.4:p.Glu561Met
NM_001304718.2:c.571_572delinsAT NP_001291647.1:p.Glu191Met
NM_000314.8:c.1162_1163delinsAT MANE Select NP_000305.3:p.Glu388Met