Canonical Allele Identifier: CA336332
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 229653

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960891del , CM000672.2:g.87960891del GRCh38
NC_000010.10:g.89720648del , CM000672.1:g.89720648del GRCh37
NC_000010.9:g.89710628del NCBI36
NG_007466.2:g.102453del , LRG_311:g.102453del

Transcript Alleles

HGVS Amino-acid change
ENST00000371953.8:c.802-3del MANE Select ENSP00000361021.3:p.=
ENST00000371953.7:c.802-3del ENSP00000361021.3:p.=
ENST00000472832.2:n.229-3del ENSP00000483066.1:p.=
NM_000314.5:c.802-3del NP_000305.3:p.=
NM_000314.6:c.802-3del NP_000305.3:p.=
NM_001304717.2:c.1321-3del NP_001291646.2:p.=
NM_001304718.1:c.211-3del NP_001291647.1:p.=
XM_006717926.2:c.757-3del XP_006717989.1:p.=
XM_011539981.1:c.802-3del XP_011538283.1:p.=
XM_011539982.1:c.706-3del XP_011538284.1:p.=
XR_945791.1:n.1372-3del
NM_000314.7:c.802-3del NP_000305.3:p.=
NM_001304717.5:c.1321-3del NP_001291646.4:p.=
NM_001304718.2:c.211-3del NP_001291647.1:p.=
NM_000314.8:c.802-3del MANE Select NP_000305.3:p.=