Canonical Allele Identifier: CA377485517
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960921A>C , CM000672.2:g.87960921A>C GRCh38
NC_000010.10:g.89720678A>C , CM000672.1:g.89720678A>C GRCh37
NC_000010.9:g.89710658A>C NCBI36
NG_007466.2:g.102483A>C , LRG_311:g.102483A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.922A>C ENSP00000514759.2:p.Thr308Pro
ENST00000710265.1:c.829A>C ENSP00000518161.1:p.Thr277Pro
ENST00000472832.3:c.829A>C ENSP00000483066.2:p.Thr277Pro
ENST00000688158.2:n.1564A>C
ENST00000688922.2:c.*659A>C ENSP00000508742.2:n.*659A>C
ENST00000700021.1:c.784A>C ENSP00000514757.1:p.Thr262Pro
ENST00000700022.1:c.*168A>C ENSP00000514758.1:n.*168A>C
ENST00000700023.1:n.1987A>C
ENST00000700024.1:n.2221A>C
ENST00000700025.1:n.1598A>C
ENST00000700026.1:n.466A>C
ENST00000700029.1:c.756A>C
ENST00000706954.1:c.829A>C ENSP00000516674.1:p.Thr277Pro
ENST00000706955.1:c.*864A>C ENSP00000516675.1:n.*864A>C
ENST00000686459.1:c.*415A>C ENSP00000508909.1:n.*415A>C
ENST00000688158.1:c.*940A>C ENSP00000509254.1:n.*940A>C
ENST00000688308.1:c.829A>C ENSP00000508752.1:p.Thr277Pro
ENST00000688922.1:c.750A>C
ENST00000693560.1:c.1348A>C ENSP00000509861.1:p.Thr450Pro
ENST00000371953.8:c.829A>C MANE Select ENSP00000361021.3:p.Thr277Pro
ENST00000371953.7:c.829A>C ENSP00000361021.3:p.Thr277Pro
ENST00000472832.2:c.256A>C ENSP00000483066.1:p.Thr86Pro
NM_000314.5:c.829A>C NP_000305.3:p.Thr277Pro
NM_000314.6:c.829A>C NP_000305.3:p.Thr277Pro
NM_001304717.2:c.1348A>C NP_001291646.2:p.Thr450Pro
NM_001304718.1:c.238A>C NP_001291647.1:p.Thr80Pro
XM_006717926.2:c.784A>C XP_006717989.1:p.Thr262Pro
XM_011539981.1:c.829A>C XP_011538283.1:p.Thr277Pro
XM_011539982.1:c.733A>C XP_011538284.1:p.Thr245Pro
XR_945791.1:n.1399A>C
NM_000314.7:c.829A>C NP_000305.3:p.Thr277Pro
NM_001304717.5:c.1348A>C NP_001291646.4:p.Thr450Pro
NM_001304718.2:c.238A>C NP_001291647.1:p.Thr80Pro
NM_000314.8:c.829A>C MANE Select NP_000305.3:p.Thr277Pro