Canonical Allele Identifier: CA2722433650
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132277936

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958038_87958039insA , CM000672.2:g.87958038_87958039insA GRCh38
NC_000010.10:g.89717795_89717796insA , CM000672.1:g.89717795_89717796insA GRCh37
NC_000010.9:g.89707775_89707776insA NCBI36
NG_007466.2:g.99600_99601insA , LRG_311:g.99600_99601insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.801+19_801+20insA ENSP00000514759.2:n.801+19_801+20insA
ENST00000710265.1:c.801+19_801+20insA ENSP00000518161.1:n.801+19_801+20insA
ENST00000472832.3:c.801+19_801+20insA ENSP00000483066.2:n.801+19_801+20insA
ENST00000688158.2:n.1536+19_1536+20insA
ENST00000688922.2:c.*631+19_*631+20insA ENSP00000508742.2:n.*631+19_*631+20insA
ENST00000700021.1:c.756+19_756+20insA ENSP00000514757.1:n.756+19_756+20insA
ENST00000700022.1:c.*140+19_*140+20insA ENSP00000514758.1:n.*140+19_*140+20insA
ENST00000700023.1:n.1959+19_1959+20insA
ENST00000700024.1:n.2193+19_2193+20insA
ENST00000700025.1:n.1570+19_1570+20insA
ENST00000700026.1:n.438+19_438+20insA
ENST00000700029.1:c.635+19_635+20insA
ENST00000706954.1:c.801+19_801+20insA ENSP00000516674.1:n.801+19_801+20insA
ENST00000706955.1:c.*836+19_*836+20insA ENSP00000516675.1:n.*836+19_*836+20insA
ENST00000686459.1:c.*387+19_*387+20insA ENSP00000508909.1:n.*387+19_*387+20insA
ENST00000688158.1:c.*912+19_*912+20insA ENSP00000509254.1:n.*912+19_*912+20insA
ENST00000688308.1:c.801+19_801+20insA ENSP00000508752.1:n.801+19_801+20insA
ENST00000688922.1:c.722+19_722+20insA
ENST00000693560.1:c.1320+19_1320+20insA ENSP00000509861.1:n.1320+19_1320+20insA
ENST00000371953.8:c.801+19_801+20insA MANE Select ENSP00000361021.3:n.801+19_801+20insA
ENST00000371953.7:c.801+19_801+20insA ENSP00000361021.3:n.801+19_801+20insA
ENST00000472832.2:c.228+19_228+20insA ENSP00000483066.1:n.228+19_228+20insA
NM_000314.5:c.801+19_801+20insA NP_000305.3:n.801+19_801+20insA
NM_000314.6:c.801+19_801+20insA NP_000305.3:n.801+19_801+20insA
NM_001304717.2:c.1320+19_1320+20insA NP_001291646.2:n.1320+19_1320+20insA
NM_001304718.1:c.210+19_210+20insA NP_001291647.1:n.210+19_210+20insA
XM_006717926.2:c.756+19_756+20insA XP_006717989.1:n.756+19_756+20insA
XM_011539981.1:c.801+19_801+20insA XP_011538283.1:n.801+19_801+20insA
XM_011539982.1:c.705+19_705+20insA XP_011538284.1:n.705+19_705+20insA
XR_945791.1:n.1371+19_1371+20insA
NM_000314.7:c.801+19_801+20insA NP_000305.3:n.801+19_801+20insA
NM_001304717.5:c.1320+19_1320+20insA NP_001291646.4:n.1320+19_1320+20insA
NM_001304718.2:c.210+19_210+20insA NP_001291647.1:n.210+19_210+20insA
NM_000314.8:c.801+19_801+20insA MANE Select NP_000305.3:n.801+19_801+20insA