Canonical Allele Identifier: CA891837789
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965390_87965391delinsTG , CM000672.2:g.87965390_87965391delinsTG GRCh38
NC_000010.10:g.89725147_89725148delinsTG , CM000672.1:g.89725147_89725148delinsTG GRCh37
NC_000010.9:g.89715127_89715128delinsTG NCBI36
NG_007466.2:g.106952_106953delinsTG , LRG_311:g.106952_106953delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1223_1224delinsTG ENSP00000514759.2:p.Tyr408Leu
ENST00000710265.1:c.*159_*160delinsTG ENSP00000518161.1:n.*159_*160delinsTG
ENST00000688158.2:n.1865_1866delinsTG
ENST00000688922.2:c.*960_*961delinsTG ENSP00000508742.2:n.*960_*961delinsTG
ENST00000700021.1:c.1085_1086delinsTG ENSP00000514757.1:p.Tyr362Leu
ENST00000700022.1:c.*469_*470delinsTG ENSP00000514758.1:n.*469_*470delinsTG
ENST00000700023.1:n.2288_2289delinsTG
ENST00000700024.1:n.2522_2523delinsTG
ENST00000706954.1:c.1130_1131delinsTG ENSP00000516674.1:p.Tyr377Leu
ENST00000706955.1:c.*1165_*1166delinsTG ENSP00000516675.1:n.*1165_*1166delinsTG
ENST00000686459.1:c.*716_*717delinsTG ENSP00000508909.1:n.*716_*717delinsTG
ENST00000688158.1:c.*1241_*1242delinsTG ENSP00000509254.1:n.*1241_*1242delinsTG
ENST00000688308.1:c.1130_1131delinsTG ENSP00000508752.1:p.Tyr377Leu
ENST00000688922.1:c.1051_1052delinsTG
ENST00000693560.1:c.1649_1650delinsTG ENSP00000509861.1:p.Tyr550Leu
ENST00000371953.8:c.1130_1131delinsTG MANE Select ENSP00000361021.3:p.Tyr377Leu
ENST00000371953.7:c.1130_1131delinsTG ENSP00000361021.3:p.Tyr377Leu
NM_000314.5:c.1130_1131delinsTG NP_000305.3:p.Tyr377Leu
NM_000314.6:c.1130_1131delinsTG NP_000305.3:p.Tyr377Leu
NM_001304717.2:c.1649_1650delinsTG NP_001291646.2:p.Tyr550Leu
NM_001304718.1:c.539_540delinsTG NP_001291647.1:p.Tyr180Leu
XM_006717926.2:c.1085_1086delinsTG XP_006717989.1:p.Tyr362Leu
XM_011539982.1:c.1034_1035delinsTG XP_011538284.1:p.Tyr345Leu
XR_945791.1:n.1700_1701delinsTG
NM_000314.7:c.1130_1131delinsTG NP_000305.3:p.Tyr377Leu
NM_001304717.5:c.1649_1650delinsTG NP_001291646.4:p.Tyr550Leu
NM_001304718.2:c.539_540delinsTG NP_001291647.1:p.Tyr180Leu
NM_000314.8:c.1130_1131delinsTG MANE Select NP_000305.3:p.Tyr377Leu