Canonical Allele Identifier: CA891839795
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957951_87957952delinsTT , CM000672.2:g.87957951_87957952delinsTT GRCh38
NC_000010.10:g.89717708_89717709delinsTT , CM000672.1:g.89717708_89717709delinsTT GRCh37
NC_000010.9:g.89707688_89707689delinsTT NCBI36
NG_007466.2:g.99513_99514delinsTT , LRG_311:g.99513_99514delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.733_734delinsTT ENSP00000514759.2:p.Gln245Leu
ENST00000710265.1:c.733_734delinsTT ENSP00000518161.1:p.Gln245Leu
ENST00000472832.3:c.733_734delinsTT ENSP00000483066.2:p.Gln245Leu
ENST00000688158.2:n.1468_1469delinsTT
ENST00000688922.2:c.*563_*564delinsTT ENSP00000508742.2:n.*563_*564delinsTT
ENST00000700021.1:c.688_689delinsTT ENSP00000514757.1:p.Gln230Leu
ENST00000700022.1:c.*72_*73delinsTT ENSP00000514758.1:n.*72_*73delinsTT
ENST00000700023.1:n.1891_1892delinsTT
ENST00000700024.1:n.2125_2126delinsTT
ENST00000700025.1:n.1502_1503delinsTT
ENST00000700026.1:n.370_371delinsTT
ENST00000700029.1:c.567_568delinsTT
ENST00000706954.1:c.733_734delinsTT ENSP00000516674.1:p.Gln245Leu
ENST00000706955.1:c.*768_*769delinsTT ENSP00000516675.1:n.*768_*769delinsTT
ENST00000686459.1:c.*319_*320delinsTT ENSP00000508909.1:n.*319_*320delinsTT
ENST00000688158.1:c.*844_*845delinsTT ENSP00000509254.1:n.*844_*845delinsTT
ENST00000688308.1:c.733_734delinsTT ENSP00000508752.1:p.Gln245Leu
ENST00000688922.1:c.654_655delinsTT
ENST00000693560.1:c.1252_1253delinsTT ENSP00000509861.1:p.Gln418Leu
ENST00000371953.8:c.733_734delinsTT MANE Select ENSP00000361021.3:p.Gln245Leu
ENST00000371953.7:c.733_734delinsTT ENSP00000361021.3:p.Gln245Leu
ENST00000472832.2:c.160_161delinsTT ENSP00000483066.1:p.Gln54Leu
NM_000314.5:c.733_734delinsTT NP_000305.3:p.Gln245Leu
NM_000314.6:c.733_734delinsTT NP_000305.3:p.Gln245Leu
NM_001304717.2:c.1252_1253delinsTT NP_001291646.2:p.Gln418Leu
NM_001304718.1:c.142_143delinsTT NP_001291647.1:p.Gln48Leu
XM_006717926.2:c.688_689delinsTT XP_006717989.1:p.Gln230Leu
XM_011539981.1:c.733_734delinsTT XP_011538283.1:p.Gln245Leu
XM_011539982.1:c.637_638delinsTT XP_011538284.1:p.Gln213Leu
XR_945791.1:n.1303_1304delinsTT
NM_000314.7:c.733_734delinsTT NP_000305.3:p.Gln245Leu
NM_001304717.5:c.1252_1253delinsTT NP_001291646.4:p.Gln418Leu
NM_001304718.2:c.142_143delinsTT NP_001291647.1:p.Gln48Leu
NM_000314.8:c.733_734delinsTT MANE Select NP_000305.3:p.Gln245Leu