Canonical Allele Identifier: CA377485616
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960948A>C , CM000672.2:g.87960948A>C GRCh38
NC_000010.10:g.89720705A>C , CM000672.1:g.89720705A>C GRCh37
NC_000010.9:g.89710685A>C NCBI36
NG_007466.2:g.102510A>C , LRG_311:g.102510A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.949A>C ENSP00000514759.2:p.Thr317Pro
ENST00000710265.1:c.856A>C ENSP00000518161.1:p.Thr286Pro
ENST00000472832.3:c.856A>C ENSP00000483066.2:p.Thr286Pro
ENST00000688158.2:n.1591A>C
ENST00000688922.2:c.*686A>C ENSP00000508742.2:n.*686A>C
ENST00000700021.1:c.811A>C ENSP00000514757.1:p.Thr271Pro
ENST00000700022.1:c.*195A>C ENSP00000514758.1:n.*195A>C
ENST00000700023.1:n.2014A>C
ENST00000700024.1:n.2248A>C
ENST00000700025.1:n.1625A>C
ENST00000700026.1:n.493A>C
ENST00000700029.1:c.783A>C
ENST00000706954.1:c.856A>C ENSP00000516674.1:p.Thr286Pro
ENST00000706955.1:c.*891A>C ENSP00000516675.1:n.*891A>C
ENST00000686459.1:c.*442A>C ENSP00000508909.1:n.*442A>C
ENST00000688158.1:c.*967A>C ENSP00000509254.1:n.*967A>C
ENST00000688308.1:c.856A>C ENSP00000508752.1:p.Thr286Pro
ENST00000688922.1:c.777A>C
ENST00000693560.1:c.1375A>C ENSP00000509861.1:p.Thr459Pro
ENST00000371953.8:c.856A>C MANE Select ENSP00000361021.3:p.Thr286Pro
ENST00000371953.7:c.856A>C ENSP00000361021.3:p.Thr286Pro
ENST00000472832.2:c.283A>C ENSP00000483066.1:p.Thr95Pro
NM_000314.5:c.856A>C NP_000305.3:p.Thr286Pro
NM_000314.6:c.856A>C NP_000305.3:p.Thr286Pro
NM_001304717.2:c.1375A>C NP_001291646.2:p.Thr459Pro
NM_001304718.1:c.265A>C NP_001291647.1:p.Thr89Pro
XM_006717926.2:c.811A>C XP_006717989.1:p.Thr271Pro
XM_011539981.1:c.856A>C XP_011538283.1:p.Thr286Pro
XM_011539982.1:c.760A>C XP_011538284.1:p.Thr254Pro
XR_945791.1:n.1426A>C
NM_000314.7:c.856A>C NP_000305.3:p.Thr286Pro
NM_001304717.5:c.1375A>C NP_001291646.4:p.Thr459Pro
NM_001304718.2:c.265A>C NP_001291647.1:p.Thr89Pro
NM_000314.8:c.856A>C MANE Select NP_000305.3:p.Thr286Pro