Canonical Allele Identifier: CA891839898
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957969_87957971delinsCAA , CM000672.2:g.87957969_87957971delinsCAA GRCh38
NC_000010.10:g.89717726_89717728delinsCAA , CM000672.1:g.89717726_89717728delinsCAA GRCh37
NC_000010.9:g.89707706_89707708delinsCAA NCBI36
NG_007466.2:g.99531_99533delinsCAA , LRG_311:g.99531_99533delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.751_753delinsCAA ENSP00000514759.2:p.Gly251Gln
ENST00000710265.1:c.751_753delinsCAA ENSP00000518161.1:p.Gly251Gln
ENST00000472832.3:c.751_753delinsCAA ENSP00000483066.2:p.Gly251Gln
ENST00000688158.2:n.1486_1488delinsCAA
ENST00000688922.2:c.*581_*583delinsCAA ENSP00000508742.2:n.*581_*583delinsCAA
ENST00000700021.1:c.706_708delinsCAA ENSP00000514757.1:p.Gly236Gln
ENST00000700022.1:c.*90_*92delinsCAA ENSP00000514758.1:n.*90_*92delinsCAA
ENST00000700023.1:n.1909_1911delinsCAA
ENST00000700024.1:n.2143_2145delinsCAA
ENST00000700025.1:n.1520_1522delinsCAA
ENST00000700026.1:n.388_390delinsCAA
ENST00000700029.1:c.585_587delinsCAA
ENST00000706954.1:c.751_753delinsCAA ENSP00000516674.1:p.Gly251Gln
ENST00000706955.1:c.*786_*788delinsCAA ENSP00000516675.1:n.*786_*788delinsCAA
ENST00000686459.1:c.*337_*339delinsCAA ENSP00000508909.1:n.*337_*339delinsCAA
ENST00000688158.1:c.*862_*864delinsCAA ENSP00000509254.1:n.*862_*864delinsCAA
ENST00000688308.1:c.751_753delinsCAA ENSP00000508752.1:p.Gly251Gln
ENST00000688922.1:c.672_674delinsCAA
ENST00000693560.1:c.1270_1272delinsCAA ENSP00000509861.1:p.Gly424Gln
ENST00000371953.8:c.751_753delinsCAA MANE Select ENSP00000361021.3:p.Gly251Gln
ENST00000371953.7:c.751_753delinsCAA ENSP00000361021.3:p.Gly251Gln
ENST00000472832.2:c.178_180delinsCAA ENSP00000483066.1:p.Gly60Gln
NM_000314.5:c.751_753delinsCAA NP_000305.3:p.Gly251Gln
NM_000314.6:c.751_753delinsCAA NP_000305.3:p.Gly251Gln
NM_001304717.2:c.1270_1272delinsCAA NP_001291646.2:p.Gly424Gln
NM_001304718.1:c.160_162delinsCAA NP_001291647.1:p.Gly54Gln
XM_006717926.2:c.706_708delinsCAA XP_006717989.1:p.Gly236Gln
XM_011539981.1:c.751_753delinsCAA XP_011538283.1:p.Gly251Gln
XM_011539982.1:c.655_657delinsCAA XP_011538284.1:p.Gly219Gln
XR_945791.1:n.1321_1323delinsCAA
NM_000314.7:c.751_753delinsCAA NP_000305.3:p.Gly251Gln
NM_001304717.5:c.1270_1272delinsCAA NP_001291646.4:p.Gly424Gln
NM_001304718.2:c.160_162delinsCAA NP_001291647.1:p.Gly54Gln
NM_000314.8:c.751_753delinsCAA MANE Select NP_000305.3:p.Gly251Gln