Canonical Allele Identifier: CA377486162
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961112T>G , CM000672.2:g.87961112T>G GRCh38
NC_000010.10:g.89720869T>G , CM000672.1:g.89720869T>G GRCh37
NC_000010.9:g.89710849T>G NCBI36
NG_007466.2:g.102674T>G , LRG_311:g.102674T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1113T>G ENSP00000514759.2:p.Asn371Lys
ENST00000710265.1:c.1020T>G ENSP00000518161.1:p.Asn340Lys
ENST00000472832.3:c.1020T>G ENSP00000483066.2:p.Asn340Lys
ENST00000688158.2:n.1755T>G
ENST00000688922.2:c.*850T>G ENSP00000508742.2:n.*850T>G
ENST00000700021.1:c.975T>G ENSP00000514757.1:p.Asn325Lys
ENST00000700022.1:c.*359T>G ENSP00000514758.1:n.*359T>G
ENST00000700023.1:n.2178T>G
ENST00000700024.1:n.2412T>G
ENST00000700025.1:n.1789T>G
ENST00000700026.1:n.657T>G
ENST00000706954.1:c.1020T>G ENSP00000516674.1:p.Asn340Lys
ENST00000706955.1:c.*1055T>G ENSP00000516675.1:n.*1055T>G
ENST00000686459.1:c.*606T>G ENSP00000508909.1:n.*606T>G
ENST00000688158.1:c.*1131T>G ENSP00000509254.1:n.*1131T>G
ENST00000688308.1:c.1020T>G ENSP00000508752.1:p.Asn340Lys
ENST00000688922.1:c.941T>G
ENST00000693560.1:c.1539T>G ENSP00000509861.1:p.Asn513Lys
ENST00000371953.8:c.1020T>G MANE Select ENSP00000361021.3:p.Asn340Lys
ENST00000371953.7:c.1020T>G ENSP00000361021.3:p.Asn340Lys
ENST00000472832.2:c.447T>G ENSP00000483066.1:p.Asn149Lys
NM_000314.5:c.1020T>G NP_000305.3:p.Asn340Lys
NM_000314.6:c.1020T>G NP_000305.3:p.Asn340Lys
NM_001304717.2:c.1539T>G NP_001291646.2:p.Asn513Lys
NM_001304718.1:c.429T>G NP_001291647.1:p.Asn143Lys
XM_006717926.2:c.975T>G XP_006717989.1:p.Asn325Lys
XM_011539981.1:c.1020T>G XP_011538283.1:p.Asn340Lys
XM_011539982.1:c.924T>G XP_011538284.1:p.Asn308Lys
XR_945791.1:n.1590T>G
NM_000314.7:c.1020T>G NP_000305.3:p.Asn340Lys
NM_001304717.5:c.1539T>G NP_001291646.4:p.Asn513Lys
NM_001304718.2:c.429T>G NP_001291647.1:p.Asn143Lys
NM_000314.8:c.1020T>G MANE Select NP_000305.3:p.Asn340Lys