Canonical Allele Identifier: CA891837788
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965390_87965391delinsGG , CM000672.2:g.87965390_87965391delinsGG GRCh38
NC_000010.10:g.89725147_89725148delinsGG , CM000672.1:g.89725147_89725148delinsGG GRCh37
NC_000010.9:g.89715127_89715128delinsGG NCBI36
NG_007466.2:g.106952_106953delinsGG , LRG_311:g.106952_106953delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1223_1224delinsGG ENSP00000514759.2:p.Tyr408Trp
ENST00000710265.1:c.*159_*160delinsGG ENSP00000518161.1:n.*159_*160delinsGG
ENST00000688158.2:n.1865_1866delinsGG
ENST00000688922.2:c.*960_*961delinsGG ENSP00000508742.2:n.*960_*961delinsGG
ENST00000700021.1:c.1085_1086delinsGG ENSP00000514757.1:p.Tyr362Trp
ENST00000700022.1:c.*469_*470delinsGG ENSP00000514758.1:n.*469_*470delinsGG
ENST00000700023.1:n.2288_2289delinsGG
ENST00000700024.1:n.2522_2523delinsGG
ENST00000706954.1:c.1130_1131delinsGG ENSP00000516674.1:p.Tyr377Trp
ENST00000706955.1:c.*1165_*1166delinsGG ENSP00000516675.1:n.*1165_*1166delinsGG
ENST00000686459.1:c.*716_*717delinsGG ENSP00000508909.1:n.*716_*717delinsGG
ENST00000688158.1:c.*1241_*1242delinsGG ENSP00000509254.1:n.*1241_*1242delinsGG
ENST00000688308.1:c.1130_1131delinsGG ENSP00000508752.1:p.Tyr377Trp
ENST00000688922.1:c.1051_1052delinsGG
ENST00000693560.1:c.1649_1650delinsGG ENSP00000509861.1:p.Tyr550Trp
ENST00000371953.8:c.1130_1131delinsGG MANE Select ENSP00000361021.3:p.Tyr377Trp
ENST00000371953.7:c.1130_1131delinsGG ENSP00000361021.3:p.Tyr377Trp
NM_000314.5:c.1130_1131delinsGG NP_000305.3:p.Tyr377Trp
NM_000314.6:c.1130_1131delinsGG NP_000305.3:p.Tyr377Trp
NM_001304717.2:c.1649_1650delinsGG NP_001291646.2:p.Tyr550Trp
NM_001304718.1:c.539_540delinsGG NP_001291647.1:p.Tyr180Trp
XM_006717926.2:c.1085_1086delinsGG XP_006717989.1:p.Tyr362Trp
XM_011539982.1:c.1034_1035delinsGG XP_011538284.1:p.Tyr345Trp
XR_945791.1:n.1700_1701delinsGG
NM_000314.7:c.1130_1131delinsGG NP_000305.3:p.Tyr377Trp
NM_001304717.5:c.1649_1650delinsGG NP_001291646.4:p.Tyr550Trp
NM_001304718.2:c.539_540delinsGG NP_001291647.1:p.Tyr180Trp
NM_000314.8:c.1130_1131delinsGG MANE Select NP_000305.3:p.Tyr377Trp