Canonical Allele Identifier: CA891841738
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965467_87965468delinsCC , CM000672.2:g.87965467_87965468delinsCC GRCh38
NC_000010.10:g.89725224_89725225delinsCC , CM000672.1:g.89725224_89725225delinsCC GRCh37
NC_000010.9:g.89715204_89715205delinsCC NCBI36
NG_007466.2:g.107029_107030delinsCC , LRG_311:g.107029_107030delinsCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1300_1301delinsCC ENSP00000514759.2:p.Val434Pro
ENST00000710265.1:c.*236_*237delinsCC ENSP00000518161.1:n.*236_*237delinsCC
ENST00000688158.2:n.1942_1943delinsCC
ENST00000688922.2:c.*1037_*1038delinsCC ENSP00000508742.2:n.*1037_*1038delinsCC
ENST00000700021.1:c.1162_1163delinsCC ENSP00000514757.1:p.Val388Pro
ENST00000700022.1:c.*546_*547delinsCC ENSP00000514758.1:n.*546_*547delinsCC
ENST00000700023.1:n.2365_2366delinsCC
ENST00000700024.1:n.2599_2600delinsCC
ENST00000706954.1:c.1207_1208delinsCC ENSP00000516674.1:p.Val403Pro
ENST00000706955.1:c.*1242_*1243delinsCC ENSP00000516675.1:n.*1242_*1243delinsCC
ENST00000686459.1:c.*793_*794delinsCC ENSP00000508909.1:n.*793_*794delinsCC
ENST00000688158.1:c.*1318_*1319delinsCC ENSP00000509254.1:n.*1318_*1319delinsCC
ENST00000688308.1:c.1207_1208delinsCC ENSP00000508752.1:p.Val403Pro
ENST00000688922.1:c.1128_1129delinsCC
ENST00000693560.1:c.1726_1727delinsCC ENSP00000509861.1:p.Val576Pro
ENST00000371953.8:c.1207_1208delinsCC MANE Select ENSP00000361021.3:p.Val403Pro
ENST00000371953.7:c.1207_1208delinsCC ENSP00000361021.3:p.Val403Pro
NM_000314.5:c.1207_1208delinsCC NP_000305.3:p.Val403Pro
NM_000314.6:c.1207_1208delinsCC NP_000305.3:p.Val403Pro
NM_001304717.2:c.1726_1727delinsCC NP_001291646.2:p.Val576Pro
NM_001304718.1:c.616_617delinsCC NP_001291647.1:p.Val206Pro
XM_006717926.2:c.1162_1163delinsCC XP_006717989.1:p.Val388Pro
XM_011539982.1:c.1111_1112delinsCC XP_011538284.1:p.Val371Pro
XR_945791.1:n.1777_1778delinsCC
NM_000314.7:c.1207_1208delinsCC NP_000305.3:p.Val403Pro
NM_001304717.5:c.1726_1727delinsCC NP_001291646.4:p.Val576Pro
NM_001304718.2:c.616_617delinsCC NP_001291647.1:p.Val206Pro
NM_000314.8:c.1207_1208delinsCC MANE Select NP_000305.3:p.Val403Pro