Canonical Allele Identifier: CA377487493
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965465A>G , CM000672.2:g.87965465A>G GRCh38
NC_000010.10:g.89725222A>G , CM000672.1:g.89725222A>G GRCh37
NC_000010.9:g.89715202A>G NCBI36
NG_007466.2:g.107027A>G , LRG_311:g.107027A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1298A>G ENSP00000514759.2:p.Lys433Arg
ENST00000710265.1:c.*234A>G ENSP00000518161.1:n.*234A>G
ENST00000688158.2:n.1940A>G
ENST00000688922.2:c.*1035A>G ENSP00000508742.2:n.*1035A>G
ENST00000700021.1:c.1160A>G ENSP00000514757.1:p.Lys387Arg
ENST00000700022.1:c.*544A>G ENSP00000514758.1:n.*544A>G
ENST00000700023.1:n.2363A>G
ENST00000700024.1:n.2597A>G
ENST00000706954.1:c.1205A>G ENSP00000516674.1:p.Lys402Arg
ENST00000706955.1:c.*1240A>G ENSP00000516675.1:n.*1240A>G
ENST00000686459.1:c.*791A>G ENSP00000508909.1:n.*791A>G
ENST00000688158.1:c.*1316A>G ENSP00000509254.1:n.*1316A>G
ENST00000688308.1:c.1205A>G ENSP00000508752.1:p.Lys402Arg
ENST00000688922.1:c.1126A>G
ENST00000693560.1:c.1724A>G ENSP00000509861.1:p.Lys575Arg
ENST00000371953.8:c.1205A>G MANE Select ENSP00000361021.3:p.Lys402Arg
ENST00000371953.7:c.1205A>G ENSP00000361021.3:p.Lys402Arg
NM_000314.5:c.1205A>G NP_000305.3:p.Lys402Arg
NM_000314.6:c.1205A>G NP_000305.3:p.Lys402Arg
NM_001304717.2:c.1724A>G NP_001291646.2:p.Lys575Arg
NM_001304718.1:c.614A>G NP_001291647.1:p.Lys205Arg
XM_006717926.2:c.1160A>G XP_006717989.1:p.Lys387Arg
XM_011539982.1:c.1109A>G XP_011538284.1:p.Lys370Arg
XR_945791.1:n.1775A>G
NM_000314.7:c.1205A>G NP_000305.3:p.Lys402Arg
NM_001304717.5:c.1724A>G NP_001291646.4:p.Lys575Arg
NM_001304718.2:c.614A>G NP_001291647.1:p.Lys205Arg
NM_000314.8:c.1205A>G MANE Select NP_000305.3:p.Lys402Arg