Canonical Allele Identifier: CA377486001
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132283181

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961053A>T , CM000672.2:g.87961053A>T GRCh38
NC_000010.10:g.89720810A>T , CM000672.1:g.89720810A>T GRCh37
NC_000010.9:g.89710790A>T NCBI36
NG_007466.2:g.102615A>T , LRG_311:g.102615A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1054A>T ENSP00000514759.2:p.Thr352Ser
ENST00000710265.1:c.961A>T ENSP00000518161.1:p.Thr321Ser
ENST00000472832.3:c.961A>T ENSP00000483066.2:p.Thr321Ser
ENST00000688158.2:n.1696A>T
ENST00000688922.2:c.*791A>T ENSP00000508742.2:n.*791A>T
ENST00000700021.1:c.916A>T ENSP00000514757.1:p.Thr306Ser
ENST00000700022.1:c.*300A>T ENSP00000514758.1:n.*300A>T
ENST00000700023.1:n.2119A>T
ENST00000700024.1:n.2353A>T
ENST00000700025.1:n.1730A>T
ENST00000700026.1:n.598A>T
ENST00000706954.1:c.961A>T ENSP00000516674.1:p.Thr321Ser
ENST00000706955.1:c.*996A>T ENSP00000516675.1:n.*996A>T
ENST00000686459.1:c.*547A>T ENSP00000508909.1:n.*547A>T
ENST00000688158.1:c.*1072A>T ENSP00000509254.1:n.*1072A>T
ENST00000688308.1:c.961A>T ENSP00000508752.1:p.Thr321Ser
ENST00000688922.1:c.882A>T
ENST00000693560.1:c.1480A>T ENSP00000509861.1:p.Thr494Ser
ENST00000371953.8:c.961A>T MANE Select ENSP00000361021.3:p.Thr321Ser
ENST00000371953.7:c.961A>T ENSP00000361021.3:p.Thr321Ser
ENST00000472832.2:c.388A>T ENSP00000483066.1:p.Thr130Ser
NM_000314.5:c.961A>T NP_000305.3:p.Thr321Ser
NM_000314.6:c.961A>T NP_000305.3:p.Thr321Ser
NM_001304717.2:c.1480A>T NP_001291646.2:p.Thr494Ser
NM_001304718.1:c.370A>T NP_001291647.1:p.Thr124Ser
XM_006717926.2:c.916A>T XP_006717989.1:p.Thr306Ser
XM_011539981.1:c.961A>T XP_011538283.1:p.Thr321Ser
XM_011539982.1:c.865A>T XP_011538284.1:p.Thr289Ser
XR_945791.1:n.1531A>T
NM_000314.7:c.961A>T NP_000305.3:p.Thr321Ser
NM_001304717.5:c.1480A>T NP_001291646.4:p.Thr494Ser
NM_001304718.2:c.370A>T NP_001291647.1:p.Thr124Ser
NM_000314.8:c.961A>T MANE Select NP_000305.3:p.Thr321Ser