Canonical Allele Identifier: CA2580082294
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 2018014
ClinVar RCV Id: RCV002861786

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957947_87957958del , CM000672.2:g.87957947_87957958del GRCh38
NC_000010.10:g.89717704_89717715del , CM000672.1:g.89717704_89717715del GRCh37
NC_000010.9:g.89707684_89707695del NCBI36
NG_007466.2:g.99509_99520del , LRG_311:g.99509_99520del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.729_740del ENSP00000514759.2:p.Phe243_Pro246del
ENST00000710265.1:c.729_740del ENSP00000518161.1:p.Phe243_Pro246del
ENST00000472832.3:c.729_740del ENSP00000483066.2:p.Phe243_Pro246del
ENST00000688158.2:n.1464_1475del
ENST00000688922.2:c.*559_*570del ENSP00000508742.2:n.*559_*570del
ENST00000700021.1:c.684_695del ENSP00000514757.1:p.Phe228_Pro231del
ENST00000700022.1:c.*68_*79del ENSP00000514758.1:n.*68_*79del
ENST00000700023.1:n.1887_1898del
ENST00000700024.1:n.2121_2132del
ENST00000700025.1:n.1498_1509del
ENST00000700026.1:n.366_377del
ENST00000700029.1:c.563_574del
ENST00000706954.1:c.729_740del ENSP00000516674.1:p.Phe243_Pro246del
ENST00000706955.1:c.*764_*775del ENSP00000516675.1:n.*764_*775del
ENST00000686459.1:c.*315_*326del ENSP00000508909.1:n.*315_*326del
ENST00000688158.1:c.*840_*851del ENSP00000509254.1:n.*840_*851del
ENST00000688308.1:c.729_740del ENSP00000508752.1:p.Phe243_Pro246del
ENST00000688922.1:c.650_661del
ENST00000693560.1:c.1248_1259del ENSP00000509861.1:p.Phe416_Pro419del
ENST00000371953.8:c.729_740del MANE Select ENSP00000361021.3:p.Phe243_Pro246del
ENST00000371953.7:c.729_740del ENSP00000361021.3:p.Phe243_Pro246del
ENST00000472832.2:c.156_167del ENSP00000483066.1:p.Phe52_Pro55del
NM_000314.5:c.729_740del NP_000305.3:p.Phe243_Pro246del
NM_000314.6:c.729_740del NP_000305.3:p.Phe243_Pro246del
NM_001304717.2:c.1248_1259del NP_001291646.2:p.Phe416_Pro419del
NM_001304718.1:c.138_149del NP_001291647.1:p.Phe46_Pro49del
XM_006717926.2:c.684_695del XP_006717989.1:p.Phe228_Pro231del
XM_011539981.1:c.729_740del XP_011538283.1:p.Phe243_Pro246del
XM_011539982.1:c.633_644del XP_011538284.1:p.Phe211_Pro214del
XR_945791.1:n.1299_1310del
NM_000314.7:c.729_740del NP_000305.3:p.Phe243_Pro246del
NM_001304717.5:c.1248_1259del NP_001291646.4:p.Phe416_Pro419del
NM_001304718.2:c.138_149del NP_001291647.1:p.Phe46_Pro49del
NM_000314.8:c.729_740del MANE Select NP_000305.3:p.Phe243_Pro246del