Canonical Allele Identifier: CA891837467
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965353_87965355delinsATT , CM000672.2:g.87965353_87965355delinsATT GRCh38
NC_000010.10:g.89725110_89725112delinsATT , CM000672.1:g.89725110_89725112delinsATT GRCh37
NC_000010.9:g.89715090_89715092delinsATT NCBI36
NG_007466.2:g.106915_106917delinsATT , LRG_311:g.106915_106917delinsATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1186_1188delinsATT ENSP00000514759.2:p.Val396Ile
ENST00000710265.1:c.*122_*124delinsATT ENSP00000518161.1:n.*122_*124delinsATT
ENST00000688158.2:n.1828_1830delinsATT
ENST00000688922.2:c.*923_*925delinsATT ENSP00000508742.2:n.*923_*925delinsATT
ENST00000700021.1:c.1048_1050delinsATT ENSP00000514757.1:p.Val350Ile
ENST00000700022.1:c.*432_*434delinsATT ENSP00000514758.1:n.*432_*434delinsATT
ENST00000700023.1:n.2251_2253delinsATT
ENST00000700024.1:n.2485_2487delinsATT
ENST00000706954.1:c.1093_1095delinsATT ENSP00000516674.1:p.Val365Ile
ENST00000706955.1:c.*1128_*1130delinsATT ENSP00000516675.1:n.*1128_*1130delinsATT
ENST00000686459.1:c.*679_*681delinsATT ENSP00000508909.1:n.*679_*681delinsATT
ENST00000688158.1:c.*1204_*1206delinsATT ENSP00000509254.1:n.*1204_*1206delinsATT
ENST00000688308.1:c.1093_1095delinsATT ENSP00000508752.1:p.Val365Ile
ENST00000688922.1:c.1014_1016delinsATT
ENST00000693560.1:c.1612_1614delinsATT ENSP00000509861.1:p.Val538Ile
ENST00000371953.8:c.1093_1095delinsATT MANE Select ENSP00000361021.3:p.Val365Ile
ENST00000371953.7:c.1093_1095delinsATT ENSP00000361021.3:p.Val365Ile
NM_000314.5:c.1093_1095delinsATT NP_000305.3:p.Val365Ile
NM_000314.6:c.1093_1095delinsATT NP_000305.3:p.Val365Ile
NM_001304717.2:c.1612_1614delinsATT NP_001291646.2:p.Val538Ile
NM_001304718.1:c.502_504delinsATT NP_001291647.1:p.Val168Ile
XM_006717926.2:c.1048_1050delinsATT XP_006717989.1:p.Val350Ile
XM_011539982.1:c.997_999delinsATT XP_011538284.1:p.Val333Ile
XR_945791.1:n.1663_1665delinsATT
NM_000314.7:c.1093_1095delinsATT NP_000305.3:p.Val365Ile
NM_001304717.5:c.1612_1614delinsATT NP_001291646.4:p.Val538Ile
NM_001304718.2:c.502_504delinsATT NP_001291647.1:p.Val168Ile
NM_000314.8:c.1093_1095delinsATT MANE Select NP_000305.3:p.Val365Ile