Canonical Allele Identifier: CA891840087
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958006_87958007delinsTT , CM000672.2:g.87958006_87958007delinsTT GRCh38
NC_000010.10:g.89717763_89717764delinsTT , CM000672.1:g.89717763_89717764delinsTT GRCh37
NC_000010.9:g.89707743_89707744delinsTT NCBI36
NG_007466.2:g.99568_99569delinsTT , LRG_311:g.99568_99569delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.788_789delinsTT ENSP00000514759.2:p.Lys263Ile
ENST00000710265.1:c.788_789delinsTT ENSP00000518161.1:p.Lys263Ile
ENST00000472832.3:c.788_789delinsTT ENSP00000483066.2:p.Lys263Ile
ENST00000688158.2:n.1523_1524delinsTT
ENST00000688922.2:c.*618_*619delinsTT ENSP00000508742.2:n.*618_*619delinsTT
ENST00000700021.1:c.743_744delinsTT ENSP00000514757.1:p.Lys248Ile
ENST00000700022.1:c.*127_*128delinsTT ENSP00000514758.1:n.*127_*128delinsTT
ENST00000700023.1:n.1946_1947delinsTT
ENST00000700024.1:n.2180_2181delinsTT
ENST00000700025.1:n.1557_1558delinsTT
ENST00000700026.1:n.425_426delinsTT
ENST00000700029.1:c.622_623delinsTT
ENST00000706954.1:c.788_789delinsTT ENSP00000516674.1:p.Lys263Ile
ENST00000706955.1:c.*823_*824delinsTT ENSP00000516675.1:n.*823_*824delinsTT
ENST00000686459.1:c.*374_*375delinsTT ENSP00000508909.1:n.*374_*375delinsTT
ENST00000688158.1:c.*899_*900delinsTT ENSP00000509254.1:n.*899_*900delinsTT
ENST00000688308.1:c.788_789delinsTT ENSP00000508752.1:p.Lys263Ile
ENST00000688922.1:c.709_710delinsTT
ENST00000693560.1:c.1307_1308delinsTT ENSP00000509861.1:p.Lys436Ile
ENST00000371953.8:c.788_789delinsTT MANE Select ENSP00000361021.3:p.Lys263Ile
ENST00000371953.7:c.788_789delinsTT ENSP00000361021.3:p.Lys263Ile
ENST00000472832.2:c.215_216delinsTT ENSP00000483066.1:p.Lys72Ile
NM_000314.5:c.788_789delinsTT NP_000305.3:p.Lys263Ile
NM_000314.6:c.788_789delinsTT NP_000305.3:p.Lys263Ile
NM_001304717.2:c.1307_1308delinsTT NP_001291646.2:p.Lys436Ile
NM_001304718.1:c.197_198delinsTT NP_001291647.1:p.Lys66Ile
XM_006717926.2:c.743_744delinsTT XP_006717989.1:p.Lys248Ile
XM_011539981.1:c.788_789delinsTT XP_011538283.1:p.Lys263Ile
XM_011539982.1:c.692_693delinsTT XP_011538284.1:p.Lys231Ile
XR_945791.1:n.1358_1359delinsTT
NM_000314.7:c.788_789delinsTT NP_000305.3:p.Lys263Ile
NM_001304717.5:c.1307_1308delinsTT NP_001291646.4:p.Lys436Ile
NM_001304718.2:c.197_198delinsTT NP_001291647.1:p.Lys66Ile
NM_000314.8:c.788_789delinsTT MANE Select NP_000305.3:p.Lys263Ile