Canonical Allele Identifier: CA891837824
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965395_87965397delinsGAA , CM000672.2:g.87965395_87965397delinsGAA GRCh38
NC_000010.10:g.89725152_89725154delinsGAA , CM000672.1:g.89725152_89725154delinsGAA GRCh37
NC_000010.9:g.89715132_89715134delinsGAA NCBI36
NG_007466.2:g.106957_106959delinsGAA , LRG_311:g.106957_106959delinsGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1228_1230delinsGAA ENSP00000514759.2:p.Tyr410Glu
ENST00000710265.1:c.*164_*166delinsGAA ENSP00000518161.1:n.*164_*166delinsGAA
ENST00000688158.2:n.1870_1872delinsGAA
ENST00000688922.2:c.*965_*967delinsGAA ENSP00000508742.2:n.*965_*967delinsGAA
ENST00000700021.1:c.1090_1092delinsGAA ENSP00000514757.1:p.Tyr364Glu
ENST00000700022.1:c.*474_*476delinsGAA ENSP00000514758.1:n.*474_*476delinsGAA
ENST00000700023.1:n.2293_2295delinsGAA
ENST00000700024.1:n.2527_2529delinsGAA
ENST00000706954.1:c.1135_1137delinsGAA ENSP00000516674.1:p.Tyr379Glu
ENST00000706955.1:c.*1170_*1172delinsGAA ENSP00000516675.1:n.*1170_*1172delinsGAA
ENST00000686459.1:c.*721_*723delinsGAA ENSP00000508909.1:n.*721_*723delinsGAA
ENST00000688158.1:c.*1246_*1248delinsGAA ENSP00000509254.1:n.*1246_*1248delinsGAA
ENST00000688308.1:c.1135_1137delinsGAA ENSP00000508752.1:p.Tyr379Glu
ENST00000688922.1:c.1056_1058delinsGAA
ENST00000693560.1:c.1654_1656delinsGAA ENSP00000509861.1:p.Tyr552Glu
ENST00000371953.8:c.1135_1137delinsGAA MANE Select ENSP00000361021.3:p.Tyr379Glu
ENST00000371953.7:c.1135_1137delinsGAA ENSP00000361021.3:p.Tyr379Glu
NM_000314.5:c.1135_1137delinsGAA NP_000305.3:p.Tyr379Glu
NM_000314.6:c.1135_1137delinsGAA NP_000305.3:p.Tyr379Glu
NM_001304717.2:c.1654_1656delinsGAA NP_001291646.2:p.Tyr552Glu
NM_001304718.1:c.544_546delinsGAA NP_001291647.1:p.Tyr182Glu
XM_006717926.2:c.1090_1092delinsGAA XP_006717989.1:p.Tyr364Glu
XM_011539982.1:c.1039_1041delinsGAA XP_011538284.1:p.Tyr347Glu
XR_945791.1:n.1705_1707delinsGAA
NM_000314.7:c.1135_1137delinsGAA NP_000305.3:p.Tyr379Glu
NM_001304717.5:c.1654_1656delinsGAA NP_001291646.4:p.Tyr552Glu
NM_001304718.2:c.544_546delinsGAA NP_001291647.1:p.Tyr182Glu
NM_000314.8:c.1135_1137delinsGAA MANE Select NP_000305.3:p.Tyr379Glu