Canonical Allele Identifier: CA377485060
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1554825247
COSMIC: COSM921132

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957996A>T , CM000672.2:g.87957996A>T GRCh38
NC_000010.10:g.89717753A>T , CM000672.1:g.89717753A>T GRCh37
NC_000010.9:g.89707733A>T NCBI36
NG_007466.2:g.99558A>T , LRG_311:g.99558A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.778A>T ENSP00000514759.2:p.Lys260Ter
ENST00000710265.1:c.778A>T ENSP00000518161.1:p.Lys260Ter
ENST00000472832.3:c.778A>T ENSP00000483066.2:p.Lys260Ter
ENST00000688158.2:n.1513A>T
ENST00000688922.2:c.*608A>T ENSP00000508742.2:n.*608A>T
ENST00000700021.1:c.733A>T ENSP00000514757.1:p.Lys245Ter
ENST00000700022.1:c.*117A>T ENSP00000514758.1:n.*117A>T
ENST00000700023.1:n.1936A>T
ENST00000700024.1:n.2170A>T
ENST00000700025.1:n.1547A>T
ENST00000700026.1:n.415A>T
ENST00000700029.1:c.612A>T
ENST00000706954.1:c.778A>T ENSP00000516674.1:p.Lys260Ter
ENST00000706955.1:c.*813A>T ENSP00000516675.1:n.*813A>T
ENST00000686459.1:c.*364A>T ENSP00000508909.1:n.*364A>T
ENST00000688158.1:c.*889A>T ENSP00000509254.1:n.*889A>T
ENST00000688308.1:c.778A>T ENSP00000508752.1:p.Lys260Ter
ENST00000688922.1:c.699A>T
ENST00000693560.1:c.1297A>T ENSP00000509861.1:p.Lys433Ter
ENST00000371953.8:c.778A>T MANE Select ENSP00000361021.3:p.Lys260Ter
ENST00000371953.7:c.778A>T ENSP00000361021.3:p.Lys260Ter
ENST00000472832.2:c.205A>T ENSP00000483066.1:p.Lys69Ter
NM_000314.5:c.778A>T NP_000305.3:p.Lys260Ter
NM_000314.6:c.778A>T NP_000305.3:p.Lys260Ter
NM_001304717.2:c.1297A>T NP_001291646.2:p.Lys433Ter
NM_001304718.1:c.187A>T NP_001291647.1:p.Lys63Ter
XM_006717926.2:c.733A>T XP_006717989.1:p.Lys245Ter
XM_011539981.1:c.778A>T XP_011538283.1:p.Lys260Ter
XM_011539982.1:c.682A>T XP_011538284.1:p.Lys228Ter
XR_945791.1:n.1348A>T
NM_000314.7:c.778A>T NP_000305.3:p.Lys260Ter
NM_001304717.5:c.1297A>T NP_001291646.4:p.Lys433Ter
NM_001304718.2:c.187A>T NP_001291647.1:p.Lys63Ter
NM_000314.8:c.778A>T MANE Select NP_000305.3:p.Lys260Ter