Canonical Allele Identifier: CA891838014
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965422_87965424delinsTGT , CM000672.2:g.87965422_87965424delinsTGT GRCh38
NC_000010.10:g.89725179_89725181delinsTGT , CM000672.1:g.89725179_89725181delinsTGT GRCh37
NC_000010.9:g.89715159_89715161delinsTGT NCBI36
NG_007466.2:g.106984_106986delinsTGT , LRG_311:g.106984_106986delinsTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1255_1257delinsTGT ENSP00000514759.2:p.Glu419Cys
ENST00000710265.1:c.*191_*193delinsTGT ENSP00000518161.1:n.*191_*193delinsTGT
ENST00000688158.2:n.1897_1899delinsTGT
ENST00000688922.2:c.*992_*994delinsTGT ENSP00000508742.2:n.*992_*994delinsTGT
ENST00000700021.1:c.1117_1119delinsTGT ENSP00000514757.1:p.Glu373Cys
ENST00000700022.1:c.*501_*503delinsTGT ENSP00000514758.1:n.*501_*503delinsTGT
ENST00000700023.1:n.2320_2322delinsTGT
ENST00000700024.1:n.2554_2556delinsTGT
ENST00000706954.1:c.1162_1164delinsTGT ENSP00000516674.1:p.Glu388Cys
ENST00000706955.1:c.*1197_*1199delinsTGT ENSP00000516675.1:n.*1197_*1199delinsTGT
ENST00000686459.1:c.*748_*750delinsTGT ENSP00000508909.1:n.*748_*750delinsTGT
ENST00000688158.1:c.*1273_*1275delinsTGT ENSP00000509254.1:n.*1273_*1275delinsTGT
ENST00000688308.1:c.1162_1164delinsTGT ENSP00000508752.1:p.Glu388Cys
ENST00000688922.1:c.1083_1085delinsTGT
ENST00000693560.1:c.1681_1683delinsTGT ENSP00000509861.1:p.Glu561Cys
ENST00000371953.8:c.1162_1164delinsTGT MANE Select ENSP00000361021.3:p.Glu388Cys
ENST00000371953.7:c.1162_1164delinsTGT ENSP00000361021.3:p.Glu388Cys
NM_000314.5:c.1162_1164delinsTGT NP_000305.3:p.Glu388Cys
NM_000314.6:c.1162_1164delinsTGT NP_000305.3:p.Glu388Cys
NM_001304717.2:c.1681_1683delinsTGT NP_001291646.2:p.Glu561Cys
NM_001304718.1:c.571_573delinsTGT NP_001291647.1:p.Glu191Cys
XM_006717926.2:c.1117_1119delinsTGT XP_006717989.1:p.Glu373Cys
XM_011539982.1:c.1066_1068delinsTGT XP_011538284.1:p.Glu356Cys
XR_945791.1:n.1732_1734delinsTGT
NM_000314.7:c.1162_1164delinsTGT NP_000305.3:p.Glu388Cys
NM_001304717.5:c.1681_1683delinsTGT NP_001291646.4:p.Glu561Cys
NM_001304718.2:c.571_573delinsTGT NP_001291647.1:p.Glu191Cys
NM_000314.8:c.1162_1164delinsTGT MANE Select NP_000305.3:p.Glu388Cys