Canonical Allele Identifier: CA891837847
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965398_87965400delinsCCA , CM000672.2:g.87965398_87965400delinsCCA GRCh38
NC_000010.10:g.89725155_89725157delinsCCA , CM000672.1:g.89725155_89725157delinsCCA GRCh37
NC_000010.9:g.89715135_89715137delinsCCA NCBI36
NG_007466.2:g.106960_106962delinsCCA , LRG_311:g.106960_106962delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1231_1233delinsCCA ENSP00000514759.2:p.Ser411Pro
ENST00000710265.1:c.*167_*169delinsCCA ENSP00000518161.1:n.*167_*169delinsCCA
ENST00000688158.2:n.1873_1875delinsCCA
ENST00000688922.2:c.*968_*970delinsCCA ENSP00000508742.2:n.*968_*970delinsCCA
ENST00000700021.1:c.1093_1095delinsCCA ENSP00000514757.1:p.Ser365Pro
ENST00000700022.1:c.*477_*479delinsCCA ENSP00000514758.1:n.*477_*479delinsCCA
ENST00000700023.1:n.2296_2298delinsCCA
ENST00000700024.1:n.2530_2532delinsCCA
ENST00000706954.1:c.1138_1140delinsCCA ENSP00000516674.1:p.Ser380Pro
ENST00000706955.1:c.*1173_*1175delinsCCA ENSP00000516675.1:n.*1173_*1175delinsCCA
ENST00000686459.1:c.*724_*726delinsCCA ENSP00000508909.1:n.*724_*726delinsCCA
ENST00000688158.1:c.*1249_*1251delinsCCA ENSP00000509254.1:n.*1249_*1251delinsCCA
ENST00000688308.1:c.1138_1140delinsCCA ENSP00000508752.1:p.Ser380Pro
ENST00000688922.1:c.1059_1061delinsCCA
ENST00000693560.1:c.1657_1659delinsCCA ENSP00000509861.1:p.Ser553Pro
ENST00000371953.8:c.1138_1140delinsCCA MANE Select ENSP00000361021.3:p.Ser380Pro
ENST00000371953.7:c.1138_1140delinsCCA ENSP00000361021.3:p.Ser380Pro
NM_000314.5:c.1138_1140delinsCCA NP_000305.3:p.Ser380Pro
NM_000314.6:c.1138_1140delinsCCA NP_000305.3:p.Ser380Pro
NM_001304717.2:c.1657_1659delinsCCA NP_001291646.2:p.Ser553Pro
NM_001304718.1:c.547_549delinsCCA NP_001291647.1:p.Ser183Pro
XM_006717926.2:c.1093_1095delinsCCA XP_006717989.1:p.Ser365Pro
XM_011539982.1:c.1042_1044delinsCCA XP_011538284.1:p.Ser348Pro
XR_945791.1:n.1708_1710delinsCCA
NM_000314.7:c.1138_1140delinsCCA NP_000305.3:p.Ser380Pro
NM_001304717.5:c.1657_1659delinsCCA NP_001291646.4:p.Ser553Pro
NM_001304718.2:c.547_549delinsCCA NP_001291647.1:p.Ser183Pro
NM_000314.8:c.1138_1140delinsCCA MANE Select NP_000305.3:p.Ser380Pro