Canonical Allele Identifier: CA891841618
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965374_87965375delinsCG , CM000672.2:g.87965374_87965375delinsCG GRCh38
NC_000010.10:g.89725131_89725132delinsCG , CM000672.1:g.89725131_89725132delinsCG GRCh37
NC_000010.9:g.89715111_89715112delinsCG NCBI36
NG_007466.2:g.106936_106937delinsCG , LRG_311:g.106936_106937delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1207_1208delinsCG ENSP00000514759.2:p.Asn403Arg
ENST00000710265.1:c.*143_*144delinsCG ENSP00000518161.1:n.*143_*144delinsCG
ENST00000688158.2:n.1849_1850delinsCG
ENST00000688922.2:c.*944_*945delinsCG ENSP00000508742.2:n.*944_*945delinsCG
ENST00000700021.1:c.1069_1070delinsCG ENSP00000514757.1:p.Asn357Arg
ENST00000700022.1:c.*453_*454delinsCG ENSP00000514758.1:n.*453_*454delinsCG
ENST00000700023.1:n.2272_2273delinsCG
ENST00000700024.1:n.2506_2507delinsCG
ENST00000706954.1:c.1114_1115delinsCG ENSP00000516674.1:p.Asn372Arg
ENST00000706955.1:c.*1149_*1150delinsCG ENSP00000516675.1:n.*1149_*1150delinsCG
ENST00000686459.1:c.*700_*701delinsCG ENSP00000508909.1:n.*700_*701delinsCG
ENST00000688158.1:c.*1225_*1226delinsCG ENSP00000509254.1:n.*1225_*1226delinsCG
ENST00000688308.1:c.1114_1115delinsCG ENSP00000508752.1:p.Asn372Arg
ENST00000688922.1:c.1035_1036delinsCG
ENST00000693560.1:c.1633_1634delinsCG ENSP00000509861.1:p.Asn545Arg
ENST00000371953.8:c.1114_1115delinsCG MANE Select ENSP00000361021.3:p.Asn372Arg
ENST00000371953.7:c.1114_1115delinsCG ENSP00000361021.3:p.Asn372Arg
NM_000314.5:c.1114_1115delinsCG NP_000305.3:p.Asn372Arg
NM_000314.6:c.1114_1115delinsCG NP_000305.3:p.Asn372Arg
NM_001304717.2:c.1633_1634delinsCG NP_001291646.2:p.Asn545Arg
NM_001304718.1:c.523_524delinsCG NP_001291647.1:p.Asn175Arg
XM_006717926.2:c.1069_1070delinsCG XP_006717989.1:p.Asn357Arg
XM_011539982.1:c.1018_1019delinsCG XP_011538284.1:p.Asn340Arg
XR_945791.1:n.1684_1685delinsCG
NM_000314.7:c.1114_1115delinsCG NP_000305.3:p.Asn372Arg
NM_001304717.5:c.1633_1634delinsCG NP_001291646.4:p.Asn545Arg
NM_001304718.2:c.523_524delinsCG NP_001291647.1:p.Asn175Arg
NM_000314.8:c.1114_1115delinsCG MANE Select NP_000305.3:p.Asn372Arg