Canonical Allele Identifier: CA2520746232
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967397_87967398insATAAAA , CM000672.2:g.87967397_87967398insATAAAA GRCh38
NC_000010.10:g.89727154_89727155insATAAAA , CM000672.1:g.89727154_89727155insATAAAA GRCh37
NC_000010.9:g.89717134_89717135insATAAAA NCBI36
NG_007466.2:g.108959_108960insATAAAA , LRG_311:g.108959_108960insATAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000710265.1:c.*2166_*2167insATAAAA ENSP00000518161.1:n.*2166_*2167insATAAAA
ENST00000688158.2:n.3872_3873insATAAAA
ENST00000706954.1:c.*1925_*1926insATAAAA ENSP00000516674.1:n.*1925_*1926insATAAAA
ENST00000706955.1:c.*3172_*3173insATAAAA ENSP00000516675.1:n.*3172_*3173insATAAAA
ENST00000688158.1:c.*3248_*3249insATAAAA ENSP00000509254.1:n.*3248_*3249insATAAAA
ENST00000693560.1:c.*1925_*1926insATAAAA ENSP00000509861.1:n.*1925_*1926insATAAAA
ENST00000371953.8:c.*1925_*1926insATAAAA MANE Select ENSP00000361021.3:n.*1925_*1926insATAAAA
ENST00000371953.7:c.*1925_*1926insATAAAA ENSP00000361021.3:n.*1925_*1926insATAAAA
NM_000314.5:c.*1925_*1926insATAAAA NP_000305.3:n.*1925_*1926insATAAAA
NM_000314.6:c.*1925_*1926insATAAAA NP_000305.3:n.*1925_*1926insATAAAA
NM_001304717.2:c.*1925_*1926insATAAAA NP_001291646.2:n.*1925_*1926insATAAAA
NM_001304718.1:c.*1925_*1926insATAAAA NP_001291647.1:n.*1925_*1926insATAAAA
XM_006717926.2:c.*1925_*1926insATAAAA XP_006717989.1:n.*1925_*1926insATAAAA
XM_011539982.1:c.*1925_*1926insATAAAA XP_011538284.1:n.*1925_*1926insATAAAA
XR_945791.1:n.3707_3708insATAAAA
NM_000314.7:c.*1925_*1926insATAAAA NP_000305.3:n.*1925_*1926insATAAAA
NM_001304717.5:c.*1925_*1926insATAAAA NP_001291646.4:n.*1925_*1926insATAAAA
NM_001304718.2:c.*1925_*1926insATAAAA NP_001291647.1:n.*1925_*1926insATAAAA
NM_000314.8:c.*1925_*1926insATAAAA MANE Select NP_000305.3:n.*1925_*1926insATAAAA