Canonical Allele Identifier: CA1926188605
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957989C= , CM000672.2:g.87957989C= GRCh38
NC_000010.10:g.89717746C= , CM000672.1:g.89717746C= GRCh37
NC_000010.9:g.89707726C= NCBI36
NG_007466.2:g.99551C= , LRG_311:g.99551C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.771C= ENSP00000514759.2:p.Phe257=
ENST00000710265.1:c.771C= ENSP00000518161.1:p.Phe257=
ENST00000472832.3:c.771C= ENSP00000483066.2:p.Phe257=
ENST00000688158.2:n.1506C=
ENST00000688922.2:c.*601C= ENSP00000508742.2:n.*601C=
ENST00000700021.1:c.726C= ENSP00000514757.1:p.Phe242=
ENST00000700022.1:c.*110C= ENSP00000514758.1:n.*110C=
ENST00000700023.1:n.1929C=
ENST00000700024.1:n.2163C=
ENST00000700025.1:n.1540C=
ENST00000700026.1:n.408C=
ENST00000700029.1:c.605C=
ENST00000706954.1:c.771C= ENSP00000516674.1:p.Phe257=
ENST00000706955.1:c.*806C= ENSP00000516675.1:n.*806C=
ENST00000686459.1:c.*357C= ENSP00000508909.1:n.*357C=
ENST00000688158.1:c.*882C= ENSP00000509254.1:n.*882C=
ENST00000688308.1:c.771C= ENSP00000508752.1:p.Phe257=
ENST00000688922.1:c.692C=
ENST00000693560.1:c.1290C= ENSP00000509861.1:p.Phe430=
ENST00000371953.8:c.771C= MANE Select ENSP00000361021.3:p.Phe257=
ENST00000371953.7:c.771C= ENSP00000361021.3:p.Phe257=
ENST00000472832.2:c.198C= ENSP00000483066.1:p.Phe66=
NM_000314.5:c.771C= NP_000305.3:p.Phe257=
NM_000314.6:c.771C= NP_000305.3:p.Phe257=
NM_001304717.2:c.1290C= NP_001291646.2:p.Phe430=
NM_001304718.1:c.180C= NP_001291647.1:p.Phe60=
XM_006717926.2:c.726C= XP_006717989.1:p.Phe242=
XM_011539981.1:c.771C= XP_011538283.1:p.Phe257=
XM_011539982.1:c.675C= XP_011538284.1:p.Phe225=
XR_945791.1:n.1341C=
NM_000314.7:c.771C= NP_000305.3:p.Phe257=
NM_001304717.5:c.1290C= NP_001291646.4:p.Phe430=
NM_001304718.2:c.180C= NP_001291647.1:p.Phe60=
NM_000314.8:c.771C= MANE Select NP_000305.3:p.Phe257=