Canonical Allele Identifier: CA2697558638
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 2717107
ClinVar RCV Id: RCV003510909

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957966dup , CM000672.2:g.87957966dup GRCh38
NC_000010.10:g.89717723dup , CM000672.1:g.89717723dup GRCh37
NC_000010.9:g.89707703dup NCBI36
NG_007466.2:g.99528dup , LRG_311:g.99528dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.748dup ENSP00000514759.2:p.Cys250LeufsTer3
ENST00000710265.1:c.748dup ENSP00000518161.1:p.Cys250LeufsTer3
ENST00000472832.3:c.748dup ENSP00000483066.2:p.Cys250LeufsTer3
ENST00000688158.2:n.1483dup
ENST00000688922.2:c.*578dup ENSP00000508742.2:n.*578dup
ENST00000700021.1:c.703dup ENSP00000514757.1:p.Cys235LeufsTer3
ENST00000700022.1:c.*87dup ENSP00000514758.1:n.*87dup
ENST00000700023.1:n.1906dup
ENST00000700024.1:n.2140dup
ENST00000700025.1:n.1517dup
ENST00000700026.1:n.385dup
ENST00000700029.1:c.582dup
ENST00000706954.1:c.748dup ENSP00000516674.1:p.Cys250LeufsTer3
ENST00000706955.1:c.*783dup ENSP00000516675.1:n.*783dup
ENST00000686459.1:c.*334dup ENSP00000508909.1:n.*334dup
ENST00000688158.1:c.*859dup ENSP00000509254.1:n.*859dup
ENST00000688308.1:c.748dup ENSP00000508752.1:p.Cys250LeufsTer3
ENST00000688922.1:c.669dup
ENST00000693560.1:c.1267dup ENSP00000509861.1:p.Cys423LeufsTer3
ENST00000371953.8:c.748dup MANE Select ENSP00000361021.3:p.Cys250LeufsTer3
ENST00000371953.7:c.748dup ENSP00000361021.3:p.Cys250LeufsTer3
ENST00000472832.2:c.175dup ENSP00000483066.1:p.Cys59LeufsTer3
NM_000314.5:c.748dup NP_000305.3:p.Cys250LeufsTer3
NM_000314.6:c.748dup NP_000305.3:p.Cys250LeufsTer3
NM_001304717.2:c.1267dup NP_001291646.2:p.Cys423LeufsTer3
NM_001304718.1:c.157dup NP_001291647.1:p.Cys53LeufsTer3
XM_006717926.2:c.703dup XP_006717989.1:p.Cys235LeufsTer3
XM_011539981.1:c.748dup XP_011538283.1:p.Cys250LeufsTer3
XM_011539982.1:c.652dup XP_011538284.1:p.Cys218LeufsTer3
XR_945791.1:n.1318dup
NM_000314.7:c.748dup NP_000305.3:p.Cys250LeufsTer3
NM_001304717.5:c.1267dup NP_001291646.4:p.Cys423LeufsTer3
NM_001304718.2:c.157dup NP_001291647.1:p.Cys53LeufsTer3
NM_000314.8:c.748dup MANE Select NP_000305.3:p.Cys250LeufsTer3