Canonical Allele Identifier: CA891839848
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957960_87957961delinsTG , CM000672.2:g.87957960_87957961delinsTG GRCh38
NC_000010.10:g.89717717_89717718delinsTG , CM000672.1:g.89717717_89717718delinsTG GRCh37
NC_000010.9:g.89707697_89707698delinsTG NCBI36
NG_007466.2:g.99522_99523delinsTG , LRG_311:g.99522_99523delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.742_743delinsTG ENSP00000514759.2:p.Pro248Cys
ENST00000710265.1:c.742_743delinsTG ENSP00000518161.1:p.Pro248Cys
ENST00000472832.3:c.742_743delinsTG ENSP00000483066.2:p.Pro248Cys
ENST00000688158.2:n.1477_1478delinsTG
ENST00000688922.2:c.*572_*573delinsTG ENSP00000508742.2:n.*572_*573delinsTG
ENST00000700021.1:c.697_698delinsTG ENSP00000514757.1:p.Pro233Cys
ENST00000700022.1:c.*81_*82delinsTG ENSP00000514758.1:n.*81_*82delinsTG
ENST00000700023.1:n.1900_1901delinsTG
ENST00000700024.1:n.2134_2135delinsTG
ENST00000700025.1:n.1511_1512delinsTG
ENST00000700026.1:n.379_380delinsTG
ENST00000700029.1:c.576_577delinsTG
ENST00000706954.1:c.742_743delinsTG ENSP00000516674.1:p.Pro248Cys
ENST00000706955.1:c.*777_*778delinsTG ENSP00000516675.1:n.*777_*778delinsTG
ENST00000686459.1:c.*328_*329delinsTG ENSP00000508909.1:n.*328_*329delinsTG
ENST00000688158.1:c.*853_*854delinsTG ENSP00000509254.1:n.*853_*854delinsTG
ENST00000688308.1:c.742_743delinsTG ENSP00000508752.1:p.Pro248Cys
ENST00000688922.1:c.663_664delinsTG
ENST00000693560.1:c.1261_1262delinsTG ENSP00000509861.1:p.Pro421Cys
ENST00000371953.8:c.742_743delinsTG MANE Select ENSP00000361021.3:p.Pro248Cys
ENST00000371953.7:c.742_743delinsTG ENSP00000361021.3:p.Pro248Cys
ENST00000472832.2:c.169_170delinsTG ENSP00000483066.1:p.Pro57Cys
NM_000314.5:c.742_743delinsTG NP_000305.3:p.Pro248Cys
NM_000314.6:c.742_743delinsTG NP_000305.3:p.Pro248Cys
NM_001304717.2:c.1261_1262delinsTG NP_001291646.2:p.Pro421Cys
NM_001304718.1:c.151_152delinsTG NP_001291647.1:p.Pro51Cys
XM_006717926.2:c.697_698delinsTG XP_006717989.1:p.Pro233Cys
XM_011539981.1:c.742_743delinsTG XP_011538283.1:p.Pro248Cys
XM_011539982.1:c.646_647delinsTG XP_011538284.1:p.Pro216Cys
XR_945791.1:n.1312_1313delinsTG
NM_000314.7:c.742_743delinsTG NP_000305.3:p.Pro248Cys
NM_001304717.5:c.1261_1262delinsTG NP_001291646.4:p.Pro421Cys
NM_001304718.2:c.151_152delinsTG NP_001291647.1:p.Pro51Cys
NM_000314.8:c.742_743delinsTG MANE Select NP_000305.3:p.Pro248Cys