Canonical Allele Identifier: CA1926190106
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961080A= , CM000672.2:g.87961080A= GRCh38
NC_000010.10:g.89720837A= , CM000672.1:g.89720837A= GRCh37
NC_000010.9:g.89710817A= NCBI36
NG_007466.2:g.102642A= , LRG_311:g.102642A=

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.1081A= ENSP00000514759.2:p.Lys361=
ENST00000710265.1:c.988A= ENSP00000518161.1:p.Lys330=
ENST00000472832.3:c.988A= ENSP00000483066.2:p.Lys330=
ENST00000688158.2:n.1723A=
ENST00000688922.2:c.*818A= ENSP00000508742.2:n.*818A=
ENST00000700021.1:c.943A= ENSP00000514757.1:p.Lys315=
ENST00000700022.1:c.*327A= ENSP00000514758.1:n.*327A=
ENST00000700023.1:n.2146A=
ENST00000700024.1:n.2380A=
ENST00000700025.1:n.1757A=
ENST00000700026.1:n.625A=
ENST00000706954.1:c.988A= ENSP00000516674.1:p.Lys330=
ENST00000706955.1:c.*1023A= ENSP00000516675.1:n.*1023A=
ENST00000686459.1:c.*574A= ENSP00000508909.1:n.*574A=
ENST00000688158.1:c.*1099A= ENSP00000509254.1:n.*1099A=
ENST00000688308.1:c.988A= ENSP00000508752.1:p.Lys330=
ENST00000688922.1:c.909A=
ENST00000693560.1:c.1507A= ENSP00000509861.1:p.Lys503=
ENST00000371953.8:c.988A= MANE Select ENSP00000361021.3:p.Lys330=
ENST00000371953.7:c.988A= ENSP00000361021.3:p.Lys330=
ENST00000472832.2:c.415A= ENSP00000483066.1:p.Lys139=
NM_000314.5:c.988A= NP_000305.3:p.Lys330=
NM_000314.6:c.988A= NP_000305.3:p.Lys330=
NM_001304717.2:c.1507A= NP_001291646.2:p.Lys503=
NM_001304718.1:c.397A= NP_001291647.1:p.Lys133=
XM_006717926.2:c.943A= XP_006717989.1:p.Lys315=
XM_011539981.1:c.988A= XP_011538283.1:p.Lys330=
XM_011539982.1:c.892A= XP_011538284.1:p.Lys298=
XR_945791.1:n.1558A=
NM_000314.7:c.988A= NP_000305.3:p.Lys330=
NM_001304717.5:c.1507A= NP_001291646.4:p.Lys503=
NM_001304718.2:c.397A= NP_001291647.1:p.Lys133=
NM_000314.8:c.988A= MANE Select NP_000305.3:p.Lys330=