Canonical Allele Identifier: CA891838018
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965422_87965423delinsTG , CM000672.2:g.87965422_87965423delinsTG GRCh38
NC_000010.10:g.89725179_89725180delinsTG , CM000672.1:g.89725179_89725180delinsTG GRCh37
NC_000010.9:g.89715159_89715160delinsTG NCBI36
NG_007466.2:g.106984_106985delinsTG , LRG_311:g.106984_106985delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1255_1256delinsTG ENSP00000514759.2:p.Glu419Trp
ENST00000710265.1:c.*191_*192delinsTG ENSP00000518161.1:n.*191_*192delinsTG
ENST00000688158.2:n.1897_1898delinsTG
ENST00000688922.2:c.*992_*993delinsTG ENSP00000508742.2:n.*992_*993delinsTG
ENST00000700021.1:c.1117_1118delinsTG ENSP00000514757.1:p.Glu373Trp
ENST00000700022.1:c.*501_*502delinsTG ENSP00000514758.1:n.*501_*502delinsTG
ENST00000700023.1:n.2320_2321delinsTG
ENST00000700024.1:n.2554_2555delinsTG
ENST00000706954.1:c.1162_1163delinsTG ENSP00000516674.1:p.Glu388Trp
ENST00000706955.1:c.*1197_*1198delinsTG ENSP00000516675.1:n.*1197_*1198delinsTG
ENST00000686459.1:c.*748_*749delinsTG ENSP00000508909.1:n.*748_*749delinsTG
ENST00000688158.1:c.*1273_*1274delinsTG ENSP00000509254.1:n.*1273_*1274delinsTG
ENST00000688308.1:c.1162_1163delinsTG ENSP00000508752.1:p.Glu388Trp
ENST00000688922.1:c.1083_1084delinsTG
ENST00000693560.1:c.1681_1682delinsTG ENSP00000509861.1:p.Glu561Trp
ENST00000371953.8:c.1162_1163delinsTG MANE Select ENSP00000361021.3:p.Glu388Trp
ENST00000371953.7:c.1162_1163delinsTG ENSP00000361021.3:p.Glu388Trp
NM_000314.5:c.1162_1163delinsTG NP_000305.3:p.Glu388Trp
NM_000314.6:c.1162_1163delinsTG NP_000305.3:p.Glu388Trp
NM_001304717.2:c.1681_1682delinsTG NP_001291646.2:p.Glu561Trp
NM_001304718.1:c.571_572delinsTG NP_001291647.1:p.Glu191Trp
XM_006717926.2:c.1117_1118delinsTG XP_006717989.1:p.Glu373Trp
XM_011539982.1:c.1066_1067delinsTG XP_011538284.1:p.Glu356Trp
XR_945791.1:n.1732_1733delinsTG
NM_000314.7:c.1162_1163delinsTG NP_000305.3:p.Glu388Trp
NM_001304717.5:c.1681_1682delinsTG NP_001291646.4:p.Glu561Trp
NM_001304718.2:c.571_572delinsTG NP_001291647.1:p.Glu191Trp
NM_000314.8:c.1162_1163delinsTG MANE Select NP_000305.3:p.Glu388Trp