Canonical Allele Identifier: CA891837830
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965395_87965397delinsCAA , CM000672.2:g.87965395_87965397delinsCAA GRCh38
NC_000010.10:g.89725152_89725154delinsCAA , CM000672.1:g.89725152_89725154delinsCAA GRCh37
NC_000010.9:g.89715132_89715134delinsCAA NCBI36
NG_007466.2:g.106957_106959delinsCAA , LRG_311:g.106957_106959delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1228_1230delinsCAA ENSP00000514759.2:p.Tyr410Gln
ENST00000710265.1:c.*164_*166delinsCAA ENSP00000518161.1:n.*164_*166delinsCAA
ENST00000688158.2:n.1870_1872delinsCAA
ENST00000688922.2:c.*965_*967delinsCAA ENSP00000508742.2:n.*965_*967delinsCAA
ENST00000700021.1:c.1090_1092delinsCAA ENSP00000514757.1:p.Tyr364Gln
ENST00000700022.1:c.*474_*476delinsCAA ENSP00000514758.1:n.*474_*476delinsCAA
ENST00000700023.1:n.2293_2295delinsCAA
ENST00000700024.1:n.2527_2529delinsCAA
ENST00000706954.1:c.1135_1137delinsCAA ENSP00000516674.1:p.Tyr379Gln
ENST00000706955.1:c.*1170_*1172delinsCAA ENSP00000516675.1:n.*1170_*1172delinsCAA
ENST00000686459.1:c.*721_*723delinsCAA ENSP00000508909.1:n.*721_*723delinsCAA
ENST00000688158.1:c.*1246_*1248delinsCAA ENSP00000509254.1:n.*1246_*1248delinsCAA
ENST00000688308.1:c.1135_1137delinsCAA ENSP00000508752.1:p.Tyr379Gln
ENST00000688922.1:c.1056_1058delinsCAA
ENST00000693560.1:c.1654_1656delinsCAA ENSP00000509861.1:p.Tyr552Gln
ENST00000371953.8:c.1135_1137delinsCAA MANE Select ENSP00000361021.3:p.Tyr379Gln
ENST00000371953.7:c.1135_1137delinsCAA ENSP00000361021.3:p.Tyr379Gln
NM_000314.5:c.1135_1137delinsCAA NP_000305.3:p.Tyr379Gln
NM_000314.6:c.1135_1137delinsCAA NP_000305.3:p.Tyr379Gln
NM_001304717.2:c.1654_1656delinsCAA NP_001291646.2:p.Tyr552Gln
NM_001304718.1:c.544_546delinsCAA NP_001291647.1:p.Tyr182Gln
XM_006717926.2:c.1090_1092delinsCAA XP_006717989.1:p.Tyr364Gln
XM_011539982.1:c.1039_1041delinsCAA XP_011538284.1:p.Tyr347Gln
XR_945791.1:n.1705_1707delinsCAA
NM_000314.7:c.1135_1137delinsCAA NP_000305.3:p.Tyr379Gln
NM_001304717.5:c.1654_1656delinsCAA NP_001291646.4:p.Tyr552Gln
NM_001304718.2:c.544_546delinsCAA NP_001291647.1:p.Tyr182Gln
NM_000314.8:c.1135_1137delinsCAA MANE Select NP_000305.3:p.Tyr379Gln