Canonical Allele Identifier: CA891837463
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965353_87965355delinsTGG , CM000672.2:g.87965353_87965355delinsTGG GRCh38
NC_000010.10:g.89725110_89725112delinsTGG , CM000672.1:g.89725110_89725112delinsTGG GRCh37
NC_000010.9:g.89715090_89715092delinsTGG NCBI36
NG_007466.2:g.106915_106917delinsTGG , LRG_311:g.106915_106917delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1186_1188delinsTGG ENSP00000514759.2:p.Val396Trp
ENST00000710265.1:c.*122_*124delinsTGG ENSP00000518161.1:n.*122_*124delinsTGG
ENST00000688158.2:n.1828_1830delinsTGG
ENST00000688922.2:c.*923_*925delinsTGG ENSP00000508742.2:n.*923_*925delinsTGG
ENST00000700021.1:c.1048_1050delinsTGG ENSP00000514757.1:p.Val350Trp
ENST00000700022.1:c.*432_*434delinsTGG ENSP00000514758.1:n.*432_*434delinsTGG
ENST00000700023.1:n.2251_2253delinsTGG
ENST00000700024.1:n.2485_2487delinsTGG
ENST00000706954.1:c.1093_1095delinsTGG ENSP00000516674.1:p.Val365Trp
ENST00000706955.1:c.*1128_*1130delinsTGG ENSP00000516675.1:n.*1128_*1130delinsTGG
ENST00000686459.1:c.*679_*681delinsTGG ENSP00000508909.1:n.*679_*681delinsTGG
ENST00000688158.1:c.*1204_*1206delinsTGG ENSP00000509254.1:n.*1204_*1206delinsTGG
ENST00000688308.1:c.1093_1095delinsTGG ENSP00000508752.1:p.Val365Trp
ENST00000688922.1:c.1014_1016delinsTGG
ENST00000693560.1:c.1612_1614delinsTGG ENSP00000509861.1:p.Val538Trp
ENST00000371953.8:c.1093_1095delinsTGG MANE Select ENSP00000361021.3:p.Val365Trp
ENST00000371953.7:c.1093_1095delinsTGG ENSP00000361021.3:p.Val365Trp
NM_000314.5:c.1093_1095delinsTGG NP_000305.3:p.Val365Trp
NM_000314.6:c.1093_1095delinsTGG NP_000305.3:p.Val365Trp
NM_001304717.2:c.1612_1614delinsTGG NP_001291646.2:p.Val538Trp
NM_001304718.1:c.502_504delinsTGG NP_001291647.1:p.Val168Trp
XM_006717926.2:c.1048_1050delinsTGG XP_006717989.1:p.Val350Trp
XM_011539982.1:c.997_999delinsTGG XP_011538284.1:p.Val333Trp
XR_945791.1:n.1663_1665delinsTGG
NM_000314.7:c.1093_1095delinsTGG NP_000305.3:p.Val365Trp
NM_001304717.5:c.1612_1614delinsTGG NP_001291646.4:p.Val538Trp
NM_001304718.2:c.502_504delinsTGG NP_001291647.1:p.Val168Trp
NM_000314.8:c.1093_1095delinsTGG MANE Select NP_000305.3:p.Val365Trp