Canonical Allele Identifier: CA1926188684
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958155_87958156delinsGT , CM000672.2:g.87958155_87958156delinsGT GRCh38
NC_000010.10:g.89717912_89717913delinsGT , CM000672.1:g.89717912_89717913delinsGT GRCh37
NC_000010.9:g.89707892_89707893delinsGT NCBI36
NG_007466.2:g.99717_99718delinsGT , LRG_311:g.99717_99718delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.801+136_801+137delinsGT ENSP00000514759.2:n.801+136_801+137delinsGT
ENST00000710265.1:c.801+136_801+137delinsGT ENSP00000518161.1:n.801+136_801+137delinsGT
ENST00000472832.3:c.801+136_801+137delinsGT ENSP00000483066.2:n.801+136_801+137delinsGT
ENST00000688158.2:n.1536+136_1536+137delinsGT
ENST00000688922.2:c.*631+136_*631+137delinsGT ENSP00000508742.2:n.*631+136_*631+137delinsGT
ENST00000700021.1:c.756+136_756+137delinsGT ENSP00000514757.1:n.756+136_756+137delinsGT
ENST00000700022.1:c.*140+136_*140+137delinsGT ENSP00000514758.1:n.*140+136_*140+137delinsGT
ENST00000700023.1:n.1959+136_1959+137delinsGT
ENST00000700024.1:n.2193+136_2193+137delinsGT
ENST00000700025.1:n.1570+136_1570+137delinsGT
ENST00000700026.1:n.438+136_438+137delinsGT
ENST00000700029.1:c.635+136_635+137delinsGT
ENST00000706954.1:c.801+136_801+137delinsGT ENSP00000516674.1:n.801+136_801+137delinsGT
ENST00000706955.1:c.*836+136_*836+137delinsGT ENSP00000516675.1:n.*836+136_*836+137delinsGT
ENST00000686459.1:c.*387+136_*387+137delinsGT ENSP00000508909.1:n.*387+136_*387+137delinsGT
ENST00000688158.1:c.*912+136_*912+137delinsGT ENSP00000509254.1:n.*912+136_*912+137delinsGT
ENST00000688308.1:c.801+136_801+137delinsGT ENSP00000508752.1:n.801+136_801+137delinsGT
ENST00000688922.1:c.722+136_722+137delinsGT
ENST00000693560.1:c.1320+136_1320+137delinsGT ENSP00000509861.1:n.1320+136_1320+137delinsGT
ENST00000371953.8:c.801+136_801+137delinsGT MANE Select ENSP00000361021.3:n.801+136_801+137delinsGT
ENST00000371953.7:c.801+136_801+137delinsGT ENSP00000361021.3:n.801+136_801+137delinsGT
ENST00000472832.2:c.228+136_228+137delinsGT ENSP00000483066.1:n.228+136_228+137delinsGT
NM_000314.5:c.801+136_801+137delinsGT NP_000305.3:n.801+136_801+137delinsGT
NM_000314.6:c.801+136_801+137delinsGT NP_000305.3:n.801+136_801+137delinsGT
NM_001304717.2:c.1320+136_1320+137delinsGT NP_001291646.2:n.1320+136_1320+137delinsGT
NM_001304718.1:c.210+136_210+137delinsGT NP_001291647.1:n.210+136_210+137delinsGT
XM_006717926.2:c.756+136_756+137delinsGT XP_006717989.1:n.756+136_756+137delinsGT
XM_011539981.1:c.801+136_801+137delinsGT XP_011538283.1:n.801+136_801+137delinsGT
XM_011539982.1:c.705+136_705+137delinsGT XP_011538284.1:n.705+136_705+137delinsGT
XR_945791.1:n.1371+136_1371+137delinsGT
NM_000314.7:c.801+136_801+137delinsGT NP_000305.3:n.801+136_801+137delinsGT
NM_001304717.5:c.1320+136_1320+137delinsGT NP_001291646.4:n.1320+136_1320+137delinsGT
NM_001304718.2:c.210+136_210+137delinsGT NP_001291647.1:n.210+136_210+137delinsGT
NM_000314.8:c.801+136_801+137delinsGT MANE Select NP_000305.3:n.801+136_801+137delinsGT