Canonical Allele Identifier: CA377486108
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132283483

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961087A>T , CM000672.2:g.87961087A>T GRCh38
NC_000010.10:g.89720844A>T , CM000672.1:g.89720844A>T GRCh37
NC_000010.9:g.89710824A>T NCBI36
NG_007466.2:g.102649A>T , LRG_311:g.102649A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1088A>T ENSP00000514759.2:p.Lys363Ile
ENST00000710265.1:c.995A>T ENSP00000518161.1:p.Lys332Ile
ENST00000472832.3:c.995A>T ENSP00000483066.2:p.Lys332Ile
ENST00000688158.2:n.1730A>T
ENST00000688922.2:c.*825A>T ENSP00000508742.2:n.*825A>T
ENST00000700021.1:c.950A>T ENSP00000514757.1:p.Lys317Ile
ENST00000700022.1:c.*334A>T ENSP00000514758.1:n.*334A>T
ENST00000700023.1:n.2153A>T
ENST00000700024.1:n.2387A>T
ENST00000700025.1:n.1764A>T
ENST00000700026.1:n.632A>T
ENST00000706954.1:c.995A>T ENSP00000516674.1:p.Lys332Ile
ENST00000706955.1:c.*1030A>T ENSP00000516675.1:n.*1030A>T
ENST00000686459.1:c.*581A>T ENSP00000508909.1:n.*581A>T
ENST00000688158.1:c.*1106A>T ENSP00000509254.1:n.*1106A>T
ENST00000688308.1:c.995A>T ENSP00000508752.1:p.Lys332Ile
ENST00000688922.1:c.916A>T
ENST00000693560.1:c.1514A>T ENSP00000509861.1:p.Lys505Ile
ENST00000371953.8:c.995A>T MANE Select ENSP00000361021.3:p.Lys332Ile
ENST00000371953.7:c.995A>T ENSP00000361021.3:p.Lys332Ile
ENST00000472832.2:c.422A>T ENSP00000483066.1:p.Lys141Ile
NM_000314.5:c.995A>T NP_000305.3:p.Lys332Ile
NM_000314.6:c.995A>T NP_000305.3:p.Lys332Ile
NM_001304717.2:c.1514A>T NP_001291646.2:p.Lys505Ile
NM_001304718.1:c.404A>T NP_001291647.1:p.Lys135Ile
XM_006717926.2:c.950A>T XP_006717989.1:p.Lys317Ile
XM_011539981.1:c.995A>T XP_011538283.1:p.Lys332Ile
XM_011539982.1:c.899A>T XP_011538284.1:p.Lys300Ile
XR_945791.1:n.1565A>T
NM_000314.7:c.995A>T NP_000305.3:p.Lys332Ile
NM_001304717.5:c.1514A>T NP_001291646.4:p.Lys505Ile
NM_001304718.2:c.404A>T NP_001291647.1:p.Lys135Ile
NM_000314.8:c.995A>T MANE Select NP_000305.3:p.Lys332Ile