Canonical Allele Identifier: CA891840954
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958005_87958006delinsGC , CM000672.2:g.87958005_87958006delinsGC GRCh38
NC_000010.10:g.89717762_89717763delinsGC , CM000672.1:g.89717762_89717763delinsGC GRCh37
NC_000010.9:g.89707742_89707743delinsGC NCBI36
NG_007466.2:g.99567_99568delinsGC , LRG_311:g.99567_99568delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.787_788delinsGC ENSP00000514759.2:p.Lys263Ala
ENST00000710265.1:c.787_788delinsGC ENSP00000518161.1:p.Lys263Ala
ENST00000472832.3:c.787_788delinsGC ENSP00000483066.2:p.Lys263Ala
ENST00000688158.2:n.1522_1523delinsGC
ENST00000688922.2:c.*617_*618delinsGC ENSP00000508742.2:n.*617_*618delinsGC
ENST00000700021.1:c.742_743delinsGC ENSP00000514757.1:p.Lys248Ala
ENST00000700022.1:c.*126_*127delinsGC ENSP00000514758.1:n.*126_*127delinsGC
ENST00000700023.1:n.1945_1946delinsGC
ENST00000700024.1:n.2179_2180delinsGC
ENST00000700025.1:n.1556_1557delinsGC
ENST00000700026.1:n.424_425delinsGC
ENST00000700029.1:c.621_622delinsGC
ENST00000706954.1:c.787_788delinsGC ENSP00000516674.1:p.Lys263Ala
ENST00000706955.1:c.*822_*823delinsGC ENSP00000516675.1:n.*822_*823delinsGC
ENST00000686459.1:c.*373_*374delinsGC ENSP00000508909.1:n.*373_*374delinsGC
ENST00000688158.1:c.*898_*899delinsGC ENSP00000509254.1:n.*898_*899delinsGC
ENST00000688308.1:c.787_788delinsGC ENSP00000508752.1:p.Lys263Ala
ENST00000688922.1:c.708_709delinsGC
ENST00000693560.1:c.1306_1307delinsGC ENSP00000509861.1:p.Lys436Ala
ENST00000371953.8:c.787_788delinsGC MANE Select ENSP00000361021.3:p.Lys263Ala
ENST00000371953.7:c.787_788delinsGC ENSP00000361021.3:p.Lys263Ala
ENST00000472832.2:c.214_215delinsGC ENSP00000483066.1:p.Lys72Ala
NM_000314.5:c.787_788delinsGC NP_000305.3:p.Lys263Ala
NM_000314.6:c.787_788delinsGC NP_000305.3:p.Lys263Ala
NM_001304717.2:c.1306_1307delinsGC NP_001291646.2:p.Lys436Ala
NM_001304718.1:c.196_197delinsGC NP_001291647.1:p.Lys66Ala
XM_006717926.2:c.742_743delinsGC XP_006717989.1:p.Lys248Ala
XM_011539981.1:c.787_788delinsGC XP_011538283.1:p.Lys263Ala
XM_011539982.1:c.691_692delinsGC XP_011538284.1:p.Lys231Ala
XR_945791.1:n.1357_1358delinsGC
NM_000314.7:c.787_788delinsGC NP_000305.3:p.Lys263Ala
NM_001304717.5:c.1306_1307delinsGC NP_001291646.4:p.Lys436Ala
NM_001304718.2:c.196_197delinsGC NP_001291647.1:p.Lys66Ala
NM_000314.8:c.787_788delinsGC MANE Select NP_000305.3:p.Lys263Ala