Canonical Allele Identifier: CA891840947
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958005_87958006delinsGT , CM000672.2:g.87958005_87958006delinsGT GRCh38
NC_000010.10:g.89717762_89717763delinsGT , CM000672.1:g.89717762_89717763delinsGT GRCh37
NC_000010.9:g.89707742_89707743delinsGT NCBI36
NG_007466.2:g.99567_99568delinsGT , LRG_311:g.99567_99568delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.787_788delinsGT ENSP00000514759.2:p.Lys263Val
ENST00000710265.1:c.787_788delinsGT ENSP00000518161.1:p.Lys263Val
ENST00000472832.3:c.787_788delinsGT ENSP00000483066.2:p.Lys263Val
ENST00000688158.2:n.1522_1523delinsGT
ENST00000688922.2:c.*617_*618delinsGT ENSP00000508742.2:n.*617_*618delinsGT
ENST00000700021.1:c.742_743delinsGT ENSP00000514757.1:p.Lys248Val
ENST00000700022.1:c.*126_*127delinsGT ENSP00000514758.1:n.*126_*127delinsGT
ENST00000700023.1:n.1945_1946delinsGT
ENST00000700024.1:n.2179_2180delinsGT
ENST00000700025.1:n.1556_1557delinsGT
ENST00000700026.1:n.424_425delinsGT
ENST00000700029.1:c.621_622delinsGT
ENST00000706954.1:c.787_788delinsGT ENSP00000516674.1:p.Lys263Val
ENST00000706955.1:c.*822_*823delinsGT ENSP00000516675.1:n.*822_*823delinsGT
ENST00000686459.1:c.*373_*374delinsGT ENSP00000508909.1:n.*373_*374delinsGT
ENST00000688158.1:c.*898_*899delinsGT ENSP00000509254.1:n.*898_*899delinsGT
ENST00000688308.1:c.787_788delinsGT ENSP00000508752.1:p.Lys263Val
ENST00000688922.1:c.708_709delinsGT
ENST00000693560.1:c.1306_1307delinsGT ENSP00000509861.1:p.Lys436Val
ENST00000371953.8:c.787_788delinsGT MANE Select ENSP00000361021.3:p.Lys263Val
ENST00000371953.7:c.787_788delinsGT ENSP00000361021.3:p.Lys263Val
ENST00000472832.2:c.214_215delinsGT ENSP00000483066.1:p.Lys72Val
NM_000314.5:c.787_788delinsGT NP_000305.3:p.Lys263Val
NM_000314.6:c.787_788delinsGT NP_000305.3:p.Lys263Val
NM_001304717.2:c.1306_1307delinsGT NP_001291646.2:p.Lys436Val
NM_001304718.1:c.196_197delinsGT NP_001291647.1:p.Lys66Val
XM_006717926.2:c.742_743delinsGT XP_006717989.1:p.Lys248Val
XM_011539981.1:c.787_788delinsGT XP_011538283.1:p.Lys263Val
XM_011539982.1:c.691_692delinsGT XP_011538284.1:p.Lys231Val
XR_945791.1:n.1357_1358delinsGT
NM_000314.7:c.787_788delinsGT NP_000305.3:p.Lys263Val
NM_001304717.5:c.1306_1307delinsGT NP_001291646.4:p.Lys436Val
NM_001304718.2:c.196_197delinsGT NP_001291647.1:p.Lys66Val
NM_000314.8:c.787_788delinsGT MANE Select NP_000305.3:p.Lys263Val