Canonical Allele Identifier: CA377484994
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132277437
COSMIC: COSM5220

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957969G>T , CM000672.2:g.87957969G>T GRCh38
NC_000010.10:g.89717726G>T , CM000672.1:g.89717726G>T GRCh37
NC_000010.9:g.89707706G>T NCBI36
NG_007466.2:g.99531G>T , LRG_311:g.99531G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.751G>T ENSP00000514759.2:p.Gly251Cys
ENST00000710265.1:c.751G>T ENSP00000518161.1:p.Gly251Cys
ENST00000472832.3:c.751G>T ENSP00000483066.2:p.Gly251Cys
ENST00000688158.2:n.1486G>T
ENST00000688922.2:c.*581G>T ENSP00000508742.2:n.*581G>T
ENST00000700021.1:c.706G>T ENSP00000514757.1:p.Gly236Cys
ENST00000700022.1:c.*90G>T ENSP00000514758.1:n.*90G>T
ENST00000700023.1:n.1909G>T
ENST00000700024.1:n.2143G>T
ENST00000700025.1:n.1520G>T
ENST00000700026.1:n.388G>T
ENST00000700029.1:c.585G>T
ENST00000706954.1:c.751G>T ENSP00000516674.1:p.Gly251Cys
ENST00000706955.1:c.*786G>T ENSP00000516675.1:n.*786G>T
ENST00000686459.1:c.*337G>T ENSP00000508909.1:n.*337G>T
ENST00000688158.1:c.*862G>T ENSP00000509254.1:n.*862G>T
ENST00000688308.1:c.751G>T ENSP00000508752.1:p.Gly251Cys
ENST00000688922.1:c.672G>T
ENST00000693560.1:c.1270G>T ENSP00000509861.1:p.Gly424Cys
ENST00000371953.8:c.751G>T MANE Select ENSP00000361021.3:p.Gly251Cys
ENST00000371953.7:c.751G>T ENSP00000361021.3:p.Gly251Cys
ENST00000472832.2:c.178G>T ENSP00000483066.1:p.Gly60Cys
NM_000314.5:c.751G>T NP_000305.3:p.Gly251Cys
NM_000314.6:c.751G>T NP_000305.3:p.Gly251Cys
NM_001304717.2:c.1270G>T NP_001291646.2:p.Gly424Cys
NM_001304718.1:c.160G>T NP_001291647.1:p.Gly54Cys
XM_006717926.2:c.706G>T XP_006717989.1:p.Gly236Cys
XM_011539981.1:c.751G>T XP_011538283.1:p.Gly251Cys
XM_011539982.1:c.655G>T XP_011538284.1:p.Gly219Cys
XR_945791.1:n.1321G>T
NM_000314.7:c.751G>T NP_000305.3:p.Gly251Cys
NM_001304717.5:c.1270G>T NP_001291646.4:p.Gly424Cys
NM_001304718.2:c.160G>T NP_001291647.1:p.Gly54Cys
NM_000314.8:c.751G>T MANE Select NP_000305.3:p.Gly251Cys