Canonical Allele Identifier: CA891837857
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965399_87965400delinsGG , CM000672.2:g.87965399_87965400delinsGG GRCh38
NC_000010.10:g.89725156_89725157delinsGG , CM000672.1:g.89725156_89725157delinsGG GRCh37
NC_000010.9:g.89715136_89715137delinsGG NCBI36
NG_007466.2:g.106961_106962delinsGG , LRG_311:g.106961_106962delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1232_1233delinsGG ENSP00000514759.2:p.Ser411Trp
ENST00000710265.1:c.*168_*169delinsGG ENSP00000518161.1:n.*168_*169delinsGG
ENST00000688158.2:n.1874_1875delinsGG
ENST00000688922.2:c.*969_*970delinsGG ENSP00000508742.2:n.*969_*970delinsGG
ENST00000700021.1:c.1094_1095delinsGG ENSP00000514757.1:p.Ser365Trp
ENST00000700022.1:c.*478_*479delinsGG ENSP00000514758.1:n.*478_*479delinsGG
ENST00000700023.1:n.2297_2298delinsGG
ENST00000700024.1:n.2531_2532delinsGG
ENST00000706954.1:c.1139_1140delinsGG ENSP00000516674.1:p.Ser380Trp
ENST00000706955.1:c.*1174_*1175delinsGG ENSP00000516675.1:n.*1174_*1175delinsGG
ENST00000686459.1:c.*725_*726delinsGG ENSP00000508909.1:n.*725_*726delinsGG
ENST00000688158.1:c.*1250_*1251delinsGG ENSP00000509254.1:n.*1250_*1251delinsGG
ENST00000688308.1:c.1139_1140delinsGG ENSP00000508752.1:p.Ser380Trp
ENST00000688922.1:c.1060_1061delinsGG
ENST00000693560.1:c.1658_1659delinsGG ENSP00000509861.1:p.Ser553Trp
ENST00000371953.8:c.1139_1140delinsGG MANE Select ENSP00000361021.3:p.Ser380Trp
ENST00000371953.7:c.1139_1140delinsGG ENSP00000361021.3:p.Ser380Trp
NM_000314.5:c.1139_1140delinsGG NP_000305.3:p.Ser380Trp
NM_000314.6:c.1139_1140delinsGG NP_000305.3:p.Ser380Trp
NM_001304717.2:c.1658_1659delinsGG NP_001291646.2:p.Ser553Trp
NM_001304718.1:c.548_549delinsGG NP_001291647.1:p.Ser183Trp
XM_006717926.2:c.1094_1095delinsGG XP_006717989.1:p.Ser365Trp
XM_011539982.1:c.1043_1044delinsGG XP_011538284.1:p.Ser348Trp
XR_945791.1:n.1709_1710delinsGG
NM_000314.7:c.1139_1140delinsGG NP_000305.3:p.Ser380Trp
NM_001304717.5:c.1658_1659delinsGG NP_001291646.4:p.Ser553Trp
NM_001304718.2:c.548_549delinsGG NP_001291647.1:p.Ser183Trp
NM_000314.8:c.1139_1140delinsGG MANE Select NP_000305.3:p.Ser380Trp