Canonical Allele Identifier: CA891840071
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958005_87958007delinsCAT , CM000672.2:g.87958005_87958007delinsCAT GRCh38
NC_000010.10:g.89717762_89717764delinsCAT , CM000672.1:g.89717762_89717764delinsCAT GRCh37
NC_000010.9:g.89707742_89707744delinsCAT NCBI36
NG_007466.2:g.99567_99569delinsCAT , LRG_311:g.99567_99569delinsCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.787_789delinsCAT ENSP00000514759.2:p.Lys263His
ENST00000710265.1:c.787_789delinsCAT ENSP00000518161.1:p.Lys263His
ENST00000472832.3:c.787_789delinsCAT ENSP00000483066.2:p.Lys263His
ENST00000688158.2:n.1522_1524delinsCAT
ENST00000688922.2:c.*617_*619delinsCAT ENSP00000508742.2:n.*617_*619delinsCAT
ENST00000700021.1:c.742_744delinsCAT ENSP00000514757.1:p.Lys248His
ENST00000700022.1:c.*126_*128delinsCAT ENSP00000514758.1:n.*126_*128delinsCAT
ENST00000700023.1:n.1945_1947delinsCAT
ENST00000700024.1:n.2179_2181delinsCAT
ENST00000700025.1:n.1556_1558delinsCAT
ENST00000700026.1:n.424_426delinsCAT
ENST00000700029.1:c.621_623delinsCAT
ENST00000706954.1:c.787_789delinsCAT ENSP00000516674.1:p.Lys263His
ENST00000706955.1:c.*822_*824delinsCAT ENSP00000516675.1:n.*822_*824delinsCAT
ENST00000686459.1:c.*373_*375delinsCAT ENSP00000508909.1:n.*373_*375delinsCAT
ENST00000688158.1:c.*898_*900delinsCAT ENSP00000509254.1:n.*898_*900delinsCAT
ENST00000688308.1:c.787_789delinsCAT ENSP00000508752.1:p.Lys263His
ENST00000688922.1:c.708_710delinsCAT
ENST00000693560.1:c.1306_1308delinsCAT ENSP00000509861.1:p.Lys436His
ENST00000371953.8:c.787_789delinsCAT MANE Select ENSP00000361021.3:p.Lys263His
ENST00000371953.7:c.787_789delinsCAT ENSP00000361021.3:p.Lys263His
ENST00000472832.2:c.214_216delinsCAT ENSP00000483066.1:p.Lys72His
NM_000314.5:c.787_789delinsCAT NP_000305.3:p.Lys263His
NM_000314.6:c.787_789delinsCAT NP_000305.3:p.Lys263His
NM_001304717.2:c.1306_1308delinsCAT NP_001291646.2:p.Lys436His
NM_001304718.1:c.196_198delinsCAT NP_001291647.1:p.Lys66His
XM_006717926.2:c.742_744delinsCAT XP_006717989.1:p.Lys248His
XM_011539981.1:c.787_789delinsCAT XP_011538283.1:p.Lys263His
XM_011539982.1:c.691_693delinsCAT XP_011538284.1:p.Lys231His
XR_945791.1:n.1357_1359delinsCAT
NM_000314.7:c.787_789delinsCAT NP_000305.3:p.Lys263His
NM_001304717.5:c.1306_1308delinsCAT NP_001291646.4:p.Lys436His
NM_001304718.2:c.196_198delinsCAT NP_001291647.1:p.Lys66His
NM_000314.8:c.787_789delinsCAT MANE Select NP_000305.3:p.Lys263His