Canonical Allele Identifier: CA891839933
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957976_87957977delinsGA , CM000672.2:g.87957976_87957977delinsGA GRCh38
NC_000010.10:g.89717733_89717734delinsGA , CM000672.1:g.89717733_89717734delinsGA GRCh37
NC_000010.9:g.89707713_89707714delinsGA NCBI36
NG_007466.2:g.99538_99539delinsGA , LRG_311:g.99538_99539delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.758_759delinsGA ENSP00000514759.2:p.Ile253Arg
ENST00000710265.1:c.758_759delinsGA ENSP00000518161.1:p.Ile253Arg
ENST00000472832.3:c.758_759delinsGA ENSP00000483066.2:p.Ile253Arg
ENST00000688158.2:n.1493_1494delinsGA
ENST00000688922.2:c.*588_*589delinsGA ENSP00000508742.2:n.*588_*589delinsGA
ENST00000700021.1:c.713_714delinsGA ENSP00000514757.1:p.Ile238Arg
ENST00000700022.1:c.*97_*98delinsGA ENSP00000514758.1:n.*97_*98delinsGA
ENST00000700023.1:n.1916_1917delinsGA
ENST00000700024.1:n.2150_2151delinsGA
ENST00000700025.1:n.1527_1528delinsGA
ENST00000700026.1:n.395_396delinsGA
ENST00000700029.1:c.592_593delinsGA
ENST00000706954.1:c.758_759delinsGA ENSP00000516674.1:p.Ile253Arg
ENST00000706955.1:c.*793_*794delinsGA ENSP00000516675.1:n.*793_*794delinsGA
ENST00000686459.1:c.*344_*345delinsGA ENSP00000508909.1:n.*344_*345delinsGA
ENST00000688158.1:c.*869_*870delinsGA ENSP00000509254.1:n.*869_*870delinsGA
ENST00000688308.1:c.758_759delinsGA ENSP00000508752.1:p.Ile253Arg
ENST00000688922.1:c.679_680delinsGA
ENST00000693560.1:c.1277_1278delinsGA ENSP00000509861.1:p.Ile426Arg
ENST00000371953.8:c.758_759delinsGA MANE Select ENSP00000361021.3:p.Ile253Arg
ENST00000371953.7:c.758_759delinsGA ENSP00000361021.3:p.Ile253Arg
ENST00000472832.2:c.185_186delinsGA ENSP00000483066.1:p.Ile62Arg
NM_000314.5:c.758_759delinsGA NP_000305.3:p.Ile253Arg
NM_000314.6:c.758_759delinsGA NP_000305.3:p.Ile253Arg
NM_001304717.2:c.1277_1278delinsGA NP_001291646.2:p.Ile426Arg
NM_001304718.1:c.167_168delinsGA NP_001291647.1:p.Ile56Arg
XM_006717926.2:c.713_714delinsGA XP_006717989.1:p.Ile238Arg
XM_011539981.1:c.758_759delinsGA XP_011538283.1:p.Ile253Arg
XM_011539982.1:c.662_663delinsGA XP_011538284.1:p.Ile221Arg
XR_945791.1:n.1328_1329delinsGA
NM_000314.7:c.758_759delinsGA NP_000305.3:p.Ile253Arg
NM_001304717.5:c.1277_1278delinsGA NP_001291646.4:p.Ile426Arg
NM_001304718.2:c.167_168delinsGA NP_001291647.1:p.Ile56Arg
NM_000314.8:c.758_759delinsGA MANE Select NP_000305.3:p.Ile253Arg