Canonical Allele Identifier: CA930911132
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87967113_87967119del , CM000672.2:g.87967113_87967119del GRCh38
NC_000010.10:g.89726870_89726876del , CM000672.1:g.89726870_89726876del GRCh37
NC_000010.9:g.89716850_89716856del NCBI36
NG_007466.2:g.108675_108681del , LRG_311:g.108675_108681del

Transcript Alleles

HGVS Amino-acid Change
ENST00000710265.1:c.*1882_*1888del ENSP00000518161.1:n.*1882_*1888del
ENST00000688158.2:n.3588_3594del
ENST00000706954.1:c.*1641_*1647del ENSP00000516674.1:n.*1641_*1647del
ENST00000706955.1:c.*2888_*2894del ENSP00000516675.1:n.*2888_*2894del
ENST00000688158.1:c.*2964_*2970del ENSP00000509254.1:n.*2964_*2970del
ENST00000693560.1:c.*1641_*1647del ENSP00000509861.1:n.*1641_*1647del
ENST00000371953.8:c.*1641_*1647del MANE Select ENSP00000361021.3:n.*1641_*1647del
ENST00000371953.7:c.*1641_*1647del ENSP00000361021.3:n.*1641_*1647del
NM_000314.5:c.*1641_*1647del NP_000305.3:n.*1641_*1647del
NM_000314.6:c.*1641_*1647del NP_000305.3:n.*1641_*1647del
NM_001304717.2:c.*1641_*1647del NP_001291646.2:n.*1641_*1647del
NM_001304718.1:c.*1641_*1647del NP_001291647.1:n.*1641_*1647del
XM_006717926.2:c.*1641_*1647del XP_006717989.1:n.*1641_*1647del
XM_011539982.1:c.*1641_*1647del XP_011538284.1:n.*1641_*1647del
XR_945791.1:n.3423_3429del
NM_000314.7:c.*1641_*1647del NP_000305.3:n.*1641_*1647del
NM_001304717.5:c.*1641_*1647del NP_001291646.4:n.*1641_*1647del
NM_001304718.2:c.*1641_*1647del NP_001291647.1:n.*1641_*1647del
NM_000314.8:c.*1641_*1647del MANE Select NP_000305.3:n.*1641_*1647del