Canonical Allele Identifier: CA645554049
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957969_87957970del , CM000672.2:g.87957969_87957970del GRCh38
NC_000010.10:g.89717726_89717727del , CM000672.1:g.89717726_89717727del GRCh37
NC_000010.9:g.89707706_89707707del NCBI36
NG_007466.2:g.99531_99532del , LRG_311:g.99531_99532del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.751_752del ENSP00000514759.2:p.Gly251Ter
ENST00000710265.1:c.751_752del ENSP00000518161.1:p.Gly251Ter
ENST00000472832.3:c.751_752del ENSP00000483066.2:p.Gly251Ter
ENST00000688158.2:n.1486_1487del
ENST00000688922.2:c.*581_*582del ENSP00000508742.2:n.*581_*582del
ENST00000700021.1:c.706_707del ENSP00000514757.1:p.Gly236Ter
ENST00000700022.1:c.*90_*91del ENSP00000514758.1:n.*90_*91del
ENST00000700023.1:n.1909_1910del
ENST00000700024.1:n.2143_2144del
ENST00000700025.1:n.1520_1521del
ENST00000700026.1:n.388_389del
ENST00000700029.1:c.585_586del
ENST00000706954.1:c.751_752del ENSP00000516674.1:p.Gly251Ter
ENST00000706955.1:c.*786_*787del ENSP00000516675.1:n.*786_*787del
ENST00000686459.1:c.*337_*338del ENSP00000508909.1:n.*337_*338del
ENST00000688158.1:c.*862_*863del ENSP00000509254.1:n.*862_*863del
ENST00000688308.1:c.751_752del ENSP00000508752.1:p.Gly251Ter
ENST00000688922.1:c.672_673del
ENST00000693560.1:c.1270_1271del ENSP00000509861.1:p.Gly424Ter
ENST00000371953.8:c.751_752del MANE Select ENSP00000361021.3:p.Gly251Ter
ENST00000371953.7:c.751_752del ENSP00000361021.3:p.Gly251Ter
ENST00000472832.2:c.178_179del ENSP00000483066.1:p.Gly60Ter
NM_000314.5:c.751_752del NP_000305.3:p.Gly251Ter
NM_000314.6:c.751_752del NP_000305.3:p.Gly251Ter
NM_001304717.2:c.1270_1271del NP_001291646.2:p.Gly424Ter
NM_001304718.1:c.160_161del NP_001291647.1:p.Gly54Ter
XM_006717926.2:c.706_707del XP_006717989.1:p.Gly236Ter
XM_011539981.1:c.751_752del XP_011538283.1:p.Gly251Ter
XM_011539982.1:c.655_656del XP_011538284.1:p.Gly219Ter
XR_945791.1:n.1321_1322del
NM_000314.7:c.751_752del NP_000305.3:p.Gly251Ter
NM_001304717.5:c.1270_1271del NP_001291646.4:p.Gly424Ter
NM_001304718.2:c.160_161del NP_001291647.1:p.Gly54Ter
NM_000314.8:c.751_752del MANE Select NP_000305.3:p.Gly251Ter