Canonical Allele Identifier: CA645553973
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM36014

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957919_87957947del , CM000672.2:g.87957919_87957947del GRCh38
NC_000010.10:g.89717676_89717704del , CM000672.1:g.89717676_89717704del GRCh37
NC_000010.9:g.89707656_89707684del NCBI36
NG_007466.2:g.99481_99509del , LRG_311:g.99481_99509del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.701_729del ENSP00000514759.2:p.Arg234ProfsTer9
ENST00000710265.1:c.701_729del ENSP00000518161.1:p.Arg234ProfsTer9
ENST00000472832.3:c.701_729del ENSP00000483066.2:p.Arg234ProfsTer9
ENST00000688158.2:n.1436_1464del
ENST00000688922.2:c.*531_*559del ENSP00000508742.2:n.*531_*559del
ENST00000700021.1:c.656_684del ENSP00000514757.1:p.Arg219ProfsTer9
ENST00000700022.1:c.*40_*68del ENSP00000514758.1:n.*40_*68del
ENST00000700023.1:n.1859_1887del
ENST00000700024.1:n.2093_2121del
ENST00000700025.1:n.1470_1498del
ENST00000700026.1:n.338_366del
ENST00000700029.1:c.535_563del
ENST00000706954.1:c.701_729del ENSP00000516674.1:p.Arg234ProfsTer9
ENST00000706955.1:c.*736_*764del ENSP00000516675.1:n.*736_*764del
ENST00000686459.1:c.*287_*315del ENSP00000508909.1:n.*287_*315del
ENST00000688158.1:c.*812_*840del ENSP00000509254.1:n.*812_*840del
ENST00000688308.1:c.701_729del ENSP00000508752.1:p.Arg234ProfsTer9
ENST00000688922.1:c.622_650del
ENST00000693560.1:c.1220_1248del ENSP00000509861.1:p.Arg407ProfsTer9
ENST00000371953.8:c.701_729del MANE Select ENSP00000361021.3:p.Arg234ProfsTer9
ENST00000371953.7:c.701_729del ENSP00000361021.3:p.Arg234ProfsTer9
ENST00000472832.2:c.128_156del ENSP00000483066.1:p.Arg43ProfsTer9
NM_000314.5:c.701_729del NP_000305.3:p.Arg234ProfsTer9
NM_000314.6:c.701_729del NP_000305.3:p.Arg234ProfsTer9
NM_001304717.2:c.1220_1248del NP_001291646.2:p.Arg407ProfsTer9
NM_001304718.1:c.110_138del NP_001291647.1:p.Arg37ProfsTer9
XM_006717926.2:c.656_684del XP_006717989.1:p.Arg219ProfsTer9
XM_011539981.1:c.701_729del XP_011538283.1:p.Arg234ProfsTer9
XM_011539982.1:c.605_633del XP_011538284.1:p.Arg202ProfsTer9
XR_945791.1:n.1271_1299del
NM_000314.7:c.701_729del NP_000305.3:p.Arg234ProfsTer9
NM_001304717.5:c.1220_1248del NP_001291646.4:p.Arg407ProfsTer9
NM_001304718.2:c.110_138del NP_001291647.1:p.Arg37ProfsTer9
NM_000314.8:c.701_729del MANE Select NP_000305.3:p.Arg234ProfsTer9