Canonical Allele Identifier: CA377486170
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961115T>A , CM000672.2:g.87961115T>A GRCh38
NC_000010.10:g.89720872T>A , CM000672.1:g.89720872T>A GRCh37
NC_000010.9:g.89710852T>A NCBI36
NG_007466.2:g.102677T>A , LRG_311:g.102677T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1116T>A ENSP00000514759.2:p.Phe372Leu
ENST00000710265.1:c.1023T>A ENSP00000518161.1:p.Phe341Leu
ENST00000472832.3:c.1023T>A ENSP00000483066.2:p.Phe341Leu
ENST00000688158.2:n.1758T>A
ENST00000688922.2:c.*853T>A ENSP00000508742.2:n.*853T>A
ENST00000700021.1:c.978T>A ENSP00000514757.1:p.Phe326Leu
ENST00000700022.1:c.*362T>A ENSP00000514758.1:n.*362T>A
ENST00000700023.1:n.2181T>A
ENST00000700024.1:n.2415T>A
ENST00000700025.1:n.1792T>A
ENST00000700026.1:n.660T>A
ENST00000706954.1:c.1023T>A ENSP00000516674.1:p.Phe341Leu
ENST00000706955.1:c.*1058T>A ENSP00000516675.1:n.*1058T>A
ENST00000686459.1:c.*609T>A ENSP00000508909.1:n.*609T>A
ENST00000688158.1:c.*1134T>A ENSP00000509254.1:n.*1134T>A
ENST00000688308.1:c.1023T>A ENSP00000508752.1:p.Phe341Leu
ENST00000688922.1:c.944T>A
ENST00000693560.1:c.1542T>A ENSP00000509861.1:p.Phe514Leu
ENST00000371953.8:c.1023T>A MANE Select ENSP00000361021.3:p.Phe341Leu
ENST00000371953.7:c.1023T>A ENSP00000361021.3:p.Phe341Leu
ENST00000472832.2:c.450T>A ENSP00000483066.1:p.Phe150Leu
NM_000314.5:c.1023T>A NP_000305.3:p.Phe341Leu
NM_000314.6:c.1023T>A NP_000305.3:p.Phe341Leu
NM_001304717.2:c.1542T>A NP_001291646.2:p.Phe514Leu
NM_001304718.1:c.432T>A NP_001291647.1:p.Phe144Leu
XM_006717926.2:c.978T>A XP_006717989.1:p.Phe326Leu
XM_011539981.1:c.1023T>A XP_011538283.1:p.Phe341Leu
XM_011539982.1:c.927T>A XP_011538284.1:p.Phe309Leu
XR_945791.1:n.1593T>A
NM_000314.7:c.1023T>A NP_000305.3:p.Phe341Leu
NM_001304717.5:c.1542T>A NP_001291646.4:p.Phe514Leu
NM_001304718.2:c.432T>A NP_001291647.1:p.Phe144Leu
NM_000314.8:c.1023T>A MANE Select NP_000305.3:p.Phe341Leu