Canonical Allele Identifier: CA1926175631
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87966842T= , CM000672.2:g.87966842T= GRCh38
NC_000010.10:g.89726599T= , CM000672.1:g.89726599T= GRCh37
NC_000010.9:g.89716579T= NCBI36
NG_007466.2:g.108404T= , LRG_311:g.108404T=

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.*1370T= ENSP00000514759.2:n.*1370T=
ENST00000710265.1:c.*1611T= ENSP00000518161.1:n.*1611T=
ENST00000688158.2:n.3317T=
ENST00000688922.2:c.*2412T= ENSP00000508742.2:n.*2412T=
ENST00000700021.1:c.*1370T= ENSP00000514757.1:n.*1370T=
ENST00000700024.1:n.3974T=
ENST00000706954.1:c.*1370T= ENSP00000516674.1:n.*1370T=
ENST00000706955.1:c.*2617T= ENSP00000516675.1:n.*2617T=
ENST00000688158.1:c.*2693T= ENSP00000509254.1:n.*2693T=
ENST00000688308.1:c.*1370T= ENSP00000508752.1:n.*1370T=
ENST00000688922.1:c.2503T=
ENST00000693560.1:c.*1370T= ENSP00000509861.1:n.*1370T=
ENST00000371953.8:c.*1370T= MANE Select ENSP00000361021.3:n.*1370T=
ENST00000371953.7:c.*1370T= ENSP00000361021.3:n.*1370T=
NM_000314.5:c.*1370T= NP_000305.3:n.*1370T=
NM_000314.6:c.*1370T= NP_000305.3:n.*1370T=
NM_001304717.2:c.*1370T= NP_001291646.2:n.*1370T=
NM_001304718.1:c.*1370T= NP_001291647.1:n.*1370T=
XM_006717926.2:c.*1370T= XP_006717989.1:n.*1370T=
XM_011539982.1:c.*1370T= XP_011538284.1:n.*1370T=
XR_945791.1:n.3152T=
NM_000314.7:c.*1370T= NP_000305.3:n.*1370T=
NM_001304717.5:c.*1370T= NP_001291646.4:n.*1370T=
NM_001304718.2:c.*1370T= NP_001291647.1:n.*1370T=
NM_000314.8:c.*1370T= MANE Select NP_000305.3:n.*1370T=