Canonical Allele Identifier: CA377485884
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1564568473

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961021A>T , CM000672.2:g.87961021A>T GRCh38
NC_000010.10:g.89720778A>T , CM000672.1:g.89720778A>T GRCh37
NC_000010.9:g.89710758A>T NCBI36
NG_007466.2:g.102583A>T , LRG_311:g.102583A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1022A>T ENSP00000514759.2:p.Asp341Val
ENST00000710265.1:c.929A>T ENSP00000518161.1:p.Asp310Val
ENST00000472832.3:c.929A>T ENSP00000483066.2:p.Asp310Val
ENST00000688158.2:n.1664A>T
ENST00000688922.2:c.*759A>T ENSP00000508742.2:n.*759A>T
ENST00000700021.1:c.884A>T ENSP00000514757.1:p.Asp295Val
ENST00000700022.1:c.*268A>T ENSP00000514758.1:n.*268A>T
ENST00000700023.1:n.2087A>T
ENST00000700024.1:n.2321A>T
ENST00000700025.1:n.1698A>T
ENST00000700026.1:n.566A>T
ENST00000706954.1:c.929A>T ENSP00000516674.1:p.Asp310Val
ENST00000706955.1:c.*964A>T ENSP00000516675.1:n.*964A>T
ENST00000686459.1:c.*515A>T ENSP00000508909.1:n.*515A>T
ENST00000688158.1:c.*1040A>T ENSP00000509254.1:n.*1040A>T
ENST00000688308.1:c.929A>T ENSP00000508752.1:p.Asp310Val
ENST00000688922.1:c.850A>T
ENST00000693560.1:c.1448A>T ENSP00000509861.1:p.Asp483Val
ENST00000371953.8:c.929A>T MANE Select ENSP00000361021.3:p.Asp310Val
ENST00000371953.7:c.929A>T ENSP00000361021.3:p.Asp310Val
ENST00000472832.2:c.356A>T ENSP00000483066.1:p.Asp119Val
NM_000314.5:c.929A>T NP_000305.3:p.Asp310Val
NM_000314.6:c.929A>T NP_000305.3:p.Asp310Val
NM_001304717.2:c.1448A>T NP_001291646.2:p.Asp483Val
NM_001304718.1:c.338A>T NP_001291647.1:p.Asp113Val
XM_006717926.2:c.884A>T XP_006717989.1:p.Asp295Val
XM_011539981.1:c.929A>T XP_011538283.1:p.Asp310Val
XM_011539982.1:c.833A>T XP_011538284.1:p.Asp278Val
XR_945791.1:n.1499A>T
NM_000314.7:c.929A>T NP_000305.3:p.Asp310Val
NM_001304717.5:c.1448A>T NP_001291646.4:p.Asp483Val
NM_001304718.2:c.338A>T NP_001291647.1:p.Asp113Val
NM_000314.8:c.929A>T MANE Select NP_000305.3:p.Asp310Val