Canonical Allele Identifier: CA377485006
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957975A>C , CM000672.2:g.87957975A>C GRCh38
NC_000010.10:g.89717732A>C , CM000672.1:g.89717732A>C GRCh37
NC_000010.9:g.89707712A>C NCBI36
NG_007466.2:g.99537A>C , LRG_311:g.99537A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.757A>C ENSP00000514759.2:p.Ile253Leu
ENST00000710265.1:c.757A>C ENSP00000518161.1:p.Ile253Leu
ENST00000472832.3:c.757A>C ENSP00000483066.2:p.Ile253Leu
ENST00000688158.2:n.1492A>C
ENST00000688922.2:c.*587A>C ENSP00000508742.2:n.*587A>C
ENST00000700021.1:c.712A>C ENSP00000514757.1:p.Ile238Leu
ENST00000700022.1:c.*96A>C ENSP00000514758.1:n.*96A>C
ENST00000700023.1:n.1915A>C
ENST00000700024.1:n.2149A>C
ENST00000700025.1:n.1526A>C
ENST00000700026.1:n.394A>C
ENST00000700029.1:c.591A>C
ENST00000706954.1:c.757A>C ENSP00000516674.1:p.Ile253Leu
ENST00000706955.1:c.*792A>C ENSP00000516675.1:n.*792A>C
ENST00000686459.1:c.*343A>C ENSP00000508909.1:n.*343A>C
ENST00000688158.1:c.*868A>C ENSP00000509254.1:n.*868A>C
ENST00000688308.1:c.757A>C ENSP00000508752.1:p.Ile253Leu
ENST00000688922.1:c.678A>C
ENST00000693560.1:c.1276A>C ENSP00000509861.1:p.Ile426Leu
ENST00000371953.8:c.757A>C MANE Select ENSP00000361021.3:p.Ile253Leu
ENST00000371953.7:c.757A>C ENSP00000361021.3:p.Ile253Leu
ENST00000472832.2:c.184A>C ENSP00000483066.1:p.Ile62Leu
NM_000314.5:c.757A>C NP_000305.3:p.Ile253Leu
NM_000314.6:c.757A>C NP_000305.3:p.Ile253Leu
NM_001304717.2:c.1276A>C NP_001291646.2:p.Ile426Leu
NM_001304718.1:c.166A>C NP_001291647.1:p.Ile56Leu
XM_006717926.2:c.712A>C XP_006717989.1:p.Ile238Leu
XM_011539981.1:c.757A>C XP_011538283.1:p.Ile253Leu
XM_011539982.1:c.661A>C XP_011538284.1:p.Ile221Leu
XR_945791.1:n.1327A>C
NM_000314.7:c.757A>C NP_000305.3:p.Ile253Leu
NM_001304717.5:c.1276A>C NP_001291646.4:p.Ile426Leu
NM_001304718.2:c.166A>C NP_001291647.1:p.Ile56Leu
NM_000314.8:c.757A>C MANE Select NP_000305.3:p.Ile253Leu