Canonical Allele Identifier: CA891840964
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958011_87958013delinsCTA , CM000672.2:g.87958011_87958013delinsCTA GRCh38
NC_000010.10:g.89717768_89717770delinsCTA , CM000672.1:g.89717768_89717770delinsCTA GRCh37
NC_000010.9:g.89707748_89707750delinsCTA NCBI36
NG_007466.2:g.99573_99575delinsCTA , LRG_311:g.99573_99575delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.793_795delinsCTA ENSP00000514759.2:p.Leu265=
ENST00000710265.1:c.793_795delinsCTA ENSP00000518161.1:p.Leu265=
ENST00000472832.3:c.793_795delinsCTA ENSP00000483066.2:p.Leu265=
ENST00000688158.2:n.1528_1530delinsCTA
ENST00000688922.2:c.*623_*625delinsCTA ENSP00000508742.2:n.*623_*625delinsCTA
ENST00000700021.1:c.748_750delinsCTA ENSP00000514757.1:p.Leu250=
ENST00000700022.1:c.*132_*134delinsCTA ENSP00000514758.1:n.*132_*134delinsCTA
ENST00000700023.1:n.1951_1953delinsCTA
ENST00000700024.1:n.2185_2187delinsCTA
ENST00000700025.1:n.1562_1564delinsCTA
ENST00000700026.1:n.430_432delinsCTA
ENST00000700029.1:c.627_629delinsCTA
ENST00000706954.1:c.793_795delinsCTA ENSP00000516674.1:p.Leu265=
ENST00000706955.1:c.*828_*830delinsCTA ENSP00000516675.1:n.*828_*830delinsCTA
ENST00000686459.1:c.*379_*381delinsCTA ENSP00000508909.1:n.*379_*381delinsCTA
ENST00000688158.1:c.*904_*906delinsCTA ENSP00000509254.1:n.*904_*906delinsCTA
ENST00000688308.1:c.793_795delinsCTA ENSP00000508752.1:p.Leu265=
ENST00000688922.1:c.714_716delinsCTA
ENST00000693560.1:c.1312_1314delinsCTA ENSP00000509861.1:p.Leu438=
ENST00000371953.8:c.793_795delinsCTA MANE Select ENSP00000361021.3:p.Leu265=
ENST00000371953.7:c.793_795delinsCTA ENSP00000361021.3:p.Leu265=
ENST00000472832.2:c.220_222delinsCTA ENSP00000483066.1:p.Leu74=
NM_000314.5:c.793_795delinsCTA NP_000305.3:p.Leu265=
NM_000314.6:c.793_795delinsCTA NP_000305.3:p.Leu265=
NM_001304717.2:c.1312_1314delinsCTA NP_001291646.2:p.Leu438=
NM_001304718.1:c.202_204delinsCTA NP_001291647.1:p.Leu68=
XM_006717926.2:c.748_750delinsCTA XP_006717989.1:p.Leu250=
XM_011539981.1:c.793_795delinsCTA XP_011538283.1:p.Leu265=
XM_011539982.1:c.697_699delinsCTA XP_011538284.1:p.Leu233=
XR_945791.1:n.1363_1365delinsCTA
NM_000314.7:c.793_795delinsCTA NP_000305.3:p.Leu265=
NM_001304717.5:c.1312_1314delinsCTA NP_001291646.4:p.Leu438=
NM_001304718.2:c.202_204delinsCTA NP_001291647.1:p.Leu68=
NM_000314.8:c.793_795delinsCTA MANE Select NP_000305.3:p.Leu265=