Canonical Allele Identifier: CA167900
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 142259
dbSNP Id: rs587782341

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957959dup , CM000672.2:g.87957959dup GRCh38
NC_000010.10:g.89717716dup , CM000672.1:g.89717716dup GRCh37
NC_000010.9:g.89707696dup NCBI36
NG_007466.2:g.99521dup , LRG_311:g.99521dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.741dup ENSP00000514759.2:p.Pro248ThrfsTer5
ENST00000710265.1:c.741dup ENSP00000518161.1:p.Pro248ThrfsTer5
ENST00000472832.3:c.741dup ENSP00000483066.2:p.Pro248ThrfsTer5
ENST00000688158.2:n.1476dup
ENST00000688922.2:c.*571dup ENSP00000508742.2:n.*571dup
ENST00000700021.1:c.696dup ENSP00000514757.1:p.Pro233ThrfsTer5
ENST00000700022.1:c.*80dup ENSP00000514758.1:n.*80dup
ENST00000700023.1:n.1899dup
ENST00000700024.1:n.2133dup
ENST00000700025.1:n.1510dup
ENST00000700026.1:n.378dup
ENST00000700029.1:c.575dup
ENST00000706954.1:c.741dup ENSP00000516674.1:p.Pro248ThrfsTer5
ENST00000706955.1:c.*776dup ENSP00000516675.1:n.*776dup
ENST00000686459.1:c.*327dup ENSP00000508909.1:n.*327dup
ENST00000688158.1:c.*852dup ENSP00000509254.1:n.*852dup
ENST00000688308.1:c.741dup ENSP00000508752.1:p.Pro248ThrfsTer5
ENST00000688922.1:c.662dup
ENST00000693560.1:c.1260dup ENSP00000509861.1:p.Pro421ThrfsTer5
ENST00000371953.8:c.741dup MANE Select ENSP00000361021.3:p.Pro248ThrfsTer5
ENST00000371953.7:c.741dup ENSP00000361021.3:p.Pro248ThrfsTer5
ENST00000472832.2:c.168dup ENSP00000483066.1:p.Pro57ThrfsTer5
NM_000314.5:c.741dup NP_000305.3:p.Pro248ThrfsTer5
NM_000314.6:c.741dup NP_000305.3:p.Pro248ThrfsTer5
NM_001304717.2:c.1260dup NP_001291646.2:p.Pro421ThrfsTer5
NM_001304718.1:c.150dup NP_001291647.1:p.Pro51ThrfsTer5
XM_006717926.2:c.696dup XP_006717989.1:p.Pro233ThrfsTer5
XM_011539981.1:c.741dup XP_011538283.1:p.Pro248ThrfsTer5
XM_011539982.1:c.645dup XP_011538284.1:p.Pro216ThrfsTer5
XR_945791.1:n.1311dup
NM_000314.7:c.741dup NP_000305.3:p.Pro248ThrfsTer5
NM_001304717.5:c.1260dup NP_001291646.4:p.Pro421ThrfsTer5
NM_001304718.2:c.150dup NP_001291647.1:p.Pro51ThrfsTer5
NM_000314.8:c.741dup MANE Select NP_000305.3:p.Pro248ThrfsTer5