Canonical Allele Identifier: CA891839804
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957951_87957952delinsTG , CM000672.2:g.87957951_87957952delinsTG GRCh38
NC_000010.10:g.89717708_89717709delinsTG , CM000672.1:g.89717708_89717709delinsTG GRCh37
NC_000010.9:g.89707688_89707689delinsTG NCBI36
NG_007466.2:g.99513_99514delinsTG , LRG_311:g.99513_99514delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.733_734delinsTG ENSP00000514759.2:p.Gln245Trp
ENST00000710265.1:c.733_734delinsTG ENSP00000518161.1:p.Gln245Trp
ENST00000472832.3:c.733_734delinsTG ENSP00000483066.2:p.Gln245Trp
ENST00000688158.2:n.1468_1469delinsTG
ENST00000688922.2:c.*563_*564delinsTG ENSP00000508742.2:n.*563_*564delinsTG
ENST00000700021.1:c.688_689delinsTG ENSP00000514757.1:p.Gln230Trp
ENST00000700022.1:c.*72_*73delinsTG ENSP00000514758.1:n.*72_*73delinsTG
ENST00000700023.1:n.1891_1892delinsTG
ENST00000700024.1:n.2125_2126delinsTG
ENST00000700025.1:n.1502_1503delinsTG
ENST00000700026.1:n.370_371delinsTG
ENST00000700029.1:c.567_568delinsTG
ENST00000706954.1:c.733_734delinsTG ENSP00000516674.1:p.Gln245Trp
ENST00000706955.1:c.*768_*769delinsTG ENSP00000516675.1:n.*768_*769delinsTG
ENST00000686459.1:c.*319_*320delinsTG ENSP00000508909.1:n.*319_*320delinsTG
ENST00000688158.1:c.*844_*845delinsTG ENSP00000509254.1:n.*844_*845delinsTG
ENST00000688308.1:c.733_734delinsTG ENSP00000508752.1:p.Gln245Trp
ENST00000688922.1:c.654_655delinsTG
ENST00000693560.1:c.1252_1253delinsTG ENSP00000509861.1:p.Gln418Trp
ENST00000371953.8:c.733_734delinsTG MANE Select ENSP00000361021.3:p.Gln245Trp
ENST00000371953.7:c.733_734delinsTG ENSP00000361021.3:p.Gln245Trp
ENST00000472832.2:c.160_161delinsTG ENSP00000483066.1:p.Gln54Trp
NM_000314.5:c.733_734delinsTG NP_000305.3:p.Gln245Trp
NM_000314.6:c.733_734delinsTG NP_000305.3:p.Gln245Trp
NM_001304717.2:c.1252_1253delinsTG NP_001291646.2:p.Gln418Trp
NM_001304718.1:c.142_143delinsTG NP_001291647.1:p.Gln48Trp
XM_006717926.2:c.688_689delinsTG XP_006717989.1:p.Gln230Trp
XM_011539981.1:c.733_734delinsTG XP_011538283.1:p.Gln245Trp
XM_011539982.1:c.637_638delinsTG XP_011538284.1:p.Gln213Trp
XR_945791.1:n.1303_1304delinsTG
NM_000314.7:c.733_734delinsTG NP_000305.3:p.Gln245Trp
NM_001304717.5:c.1252_1253delinsTG NP_001291646.4:p.Gln418Trp
NM_001304718.2:c.142_143delinsTG NP_001291647.1:p.Gln48Trp
NM_000314.8:c.733_734delinsTG MANE Select NP_000305.3:p.Gln245Trp