Canonical Allele Identifier: CA1926190047
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961020G= , CM000672.2:g.87961020G= GRCh38
NC_000010.10:g.89720777G= , CM000672.1:g.89720777G= GRCh37
NC_000010.9:g.89710757G= NCBI36
NG_007466.2:g.102582G= , LRG_311:g.102582G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1021G= ENSP00000514759.2:p.Asp341=
ENST00000710265.1:c.928G= ENSP00000518161.1:p.Asp310=
ENST00000472832.3:c.928G= ENSP00000483066.2:p.Asp310=
ENST00000688158.2:n.1663G=
ENST00000688922.2:c.*758G= ENSP00000508742.2:n.*758G=
ENST00000700021.1:c.883G= ENSP00000514757.1:p.Asp295=
ENST00000700022.1:c.*267G= ENSP00000514758.1:n.*267G=
ENST00000700023.1:n.2086G=
ENST00000700024.1:n.2320G=
ENST00000700025.1:n.1697G=
ENST00000700026.1:n.565G=
ENST00000706954.1:c.928G= ENSP00000516674.1:p.Asp310=
ENST00000706955.1:c.*963G= ENSP00000516675.1:n.*963G=
ENST00000686459.1:c.*514G= ENSP00000508909.1:n.*514G=
ENST00000688158.1:c.*1039G= ENSP00000509254.1:n.*1039G=
ENST00000688308.1:c.928G= ENSP00000508752.1:p.Asp310=
ENST00000688922.1:c.849G=
ENST00000693560.1:c.1447G= ENSP00000509861.1:p.Asp483=
ENST00000371953.8:c.928G= MANE Select ENSP00000361021.3:p.Asp310=
ENST00000371953.7:c.928G= ENSP00000361021.3:p.Asp310=
ENST00000472832.2:c.355G= ENSP00000483066.1:p.Asp119=
NM_000314.5:c.928G= NP_000305.3:p.Asp310=
NM_000314.6:c.928G= NP_000305.3:p.Asp310=
NM_001304717.2:c.1447G= NP_001291646.2:p.Asp483=
NM_001304718.1:c.337G= NP_001291647.1:p.Asp113=
XM_006717926.2:c.883G= XP_006717989.1:p.Asp295=
XM_011539981.1:c.928G= XP_011538283.1:p.Asp310=
XM_011539982.1:c.832G= XP_011538284.1:p.Asp278=
XR_945791.1:n.1498G=
NM_000314.7:c.928G= NP_000305.3:p.Asp310=
NM_001304717.5:c.1447G= NP_001291646.4:p.Asp483=
NM_001304718.2:c.337G= NP_001291647.1:p.Asp113=
NM_000314.8:c.928G= MANE Select NP_000305.3:p.Asp310=