Canonical Allele Identifier: CA891837568
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965368_87965370delinsTGG , CM000672.2:g.87965368_87965370delinsTGG GRCh38
NC_000010.10:g.89725125_89725127delinsTGG , CM000672.1:g.89725125_89725127delinsTGG GRCh37
NC_000010.9:g.89715105_89715107delinsTGG NCBI36
NG_007466.2:g.106930_106932delinsTGG , LRG_311:g.106930_106932delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1201_1203delinsTGG ENSP00000514759.2:p.Ser401Trp
ENST00000710265.1:c.*137_*139delinsTGG ENSP00000518161.1:n.*137_*139delinsTGG
ENST00000688158.2:n.1843_1845delinsTGG
ENST00000688922.2:c.*938_*940delinsTGG ENSP00000508742.2:n.*938_*940delinsTGG
ENST00000700021.1:c.1063_1065delinsTGG ENSP00000514757.1:p.Ser355Trp
ENST00000700022.1:c.*447_*449delinsTGG ENSP00000514758.1:n.*447_*449delinsTGG
ENST00000700023.1:n.2266_2268delinsTGG
ENST00000700024.1:n.2500_2502delinsTGG
ENST00000706954.1:c.1108_1110delinsTGG ENSP00000516674.1:p.Ser370Trp
ENST00000706955.1:c.*1143_*1145delinsTGG ENSP00000516675.1:n.*1143_*1145delinsTGG
ENST00000686459.1:c.*694_*696delinsTGG ENSP00000508909.1:n.*694_*696delinsTGG
ENST00000688158.1:c.*1219_*1221delinsTGG ENSP00000509254.1:n.*1219_*1221delinsTGG
ENST00000688308.1:c.1108_1110delinsTGG ENSP00000508752.1:p.Ser370Trp
ENST00000688922.1:c.1029_1031delinsTGG
ENST00000693560.1:c.1627_1629delinsTGG ENSP00000509861.1:p.Ser543Trp
ENST00000371953.8:c.1108_1110delinsTGG MANE Select ENSP00000361021.3:p.Ser370Trp
ENST00000371953.7:c.1108_1110delinsTGG ENSP00000361021.3:p.Ser370Trp
NM_000314.5:c.1108_1110delinsTGG NP_000305.3:p.Ser370Trp
NM_000314.6:c.1108_1110delinsTGG NP_000305.3:p.Ser370Trp
NM_001304717.2:c.1627_1629delinsTGG NP_001291646.2:p.Ser543Trp
NM_001304718.1:c.517_519delinsTGG NP_001291647.1:p.Ser173Trp
XM_006717926.2:c.1063_1065delinsTGG XP_006717989.1:p.Ser355Trp
XM_011539982.1:c.1012_1014delinsTGG XP_011538284.1:p.Ser338Trp
XR_945791.1:n.1678_1680delinsTGG
NM_000314.7:c.1108_1110delinsTGG NP_000305.3:p.Ser370Trp
NM_001304717.5:c.1627_1629delinsTGG NP_001291646.4:p.Ser543Trp
NM_001304718.2:c.517_519delinsTGG NP_001291647.1:p.Ser173Trp
NM_000314.8:c.1108_1110delinsTGG MANE Select NP_000305.3:p.Ser370Trp