Canonical Allele Identifier: CA2695200883
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 2674353
ClinVar RCV Id: RCV003452549

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957955del , CM000672.2:g.87957955del GRCh38
NC_000010.10:g.89717712del , CM000672.1:g.89717712del GRCh37
NC_000010.9:g.89707692del NCBI36
NG_007466.2:g.99517del , LRG_311:g.99517del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.737del ENSP00000514759.2:p.Pro246ArgfsTer10
ENST00000710265.1:c.737del ENSP00000518161.1:p.Pro246ArgfsTer10
ENST00000472832.3:c.737del ENSP00000483066.2:p.Pro246ArgfsTer10
ENST00000688158.2:n.1472del
ENST00000688922.2:c.*567del ENSP00000508742.2:n.*567del
ENST00000700021.1:c.692del ENSP00000514757.1:p.Pro231ArgfsTer10
ENST00000700022.1:c.*76del ENSP00000514758.1:n.*76del
ENST00000700023.1:n.1895del
ENST00000700024.1:n.2129del
ENST00000700025.1:n.1506del
ENST00000700026.1:n.374del
ENST00000700029.1:c.571del
ENST00000706954.1:c.737del ENSP00000516674.1:p.Pro246ArgfsTer10
ENST00000706955.1:c.*772del ENSP00000516675.1:n.*772del
ENST00000686459.1:c.*323del ENSP00000508909.1:n.*323del
ENST00000688158.1:c.*848del ENSP00000509254.1:n.*848del
ENST00000688308.1:c.737del ENSP00000508752.1:p.Pro246ArgfsTer10
ENST00000688922.1:c.658del
ENST00000693560.1:c.1256del ENSP00000509861.1:p.Pro419ArgfsTer10
ENST00000371953.8:c.737del MANE Select ENSP00000361021.3:p.Pro246ArgfsTer10
ENST00000371953.7:c.737del ENSP00000361021.3:p.Pro246ArgfsTer10
ENST00000472832.2:c.164del ENSP00000483066.1:p.Pro55ArgfsTer10
NM_000314.5:c.737del NP_000305.3:p.Pro246ArgfsTer10
NM_000314.6:c.737del NP_000305.3:p.Pro246ArgfsTer10
NM_001304717.2:c.1256del NP_001291646.2:p.Pro419ArgfsTer10
NM_001304718.1:c.146del NP_001291647.1:p.Pro49ArgfsTer10
XM_006717926.2:c.692del XP_006717989.1:p.Pro231ArgfsTer10
XM_011539981.1:c.737del XP_011538283.1:p.Pro246ArgfsTer10
XM_011539982.1:c.641del XP_011538284.1:p.Pro214ArgfsTer10
XR_945791.1:n.1307del
NM_000314.7:c.737del NP_000305.3:p.Pro246ArgfsTer10
NM_001304717.5:c.1256del NP_001291646.4:p.Pro419ArgfsTer10
NM_001304718.2:c.146del NP_001291647.1:p.Pro49ArgfsTer10
NM_000314.8:c.737del MANE Select NP_000305.3:p.Pro246ArgfsTer10