Canonical Allele Identifier: CA377486125
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs121909231
COSMIC: COSM921156

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961095C>G , CM000672.2:g.87961095C>G GRCh38
NC_000010.10:g.89720852C>G , CM000672.1:g.89720852C>G GRCh37
NC_000010.9:g.89710832C>G NCBI36
NG_007466.2:g.102657C>G , LRG_311:g.102657C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.1096C>G ENSP00000514759.2:p.Arg366Gly
ENST00000710265.1:c.1003C>G ENSP00000518161.1:p.Arg335Gly
ENST00000472832.3:c.1003C>G ENSP00000483066.2:p.Arg335Gly
ENST00000688158.2:n.1738C>G
ENST00000688922.2:c.*833C>G ENSP00000508742.2:n.*833C>G
ENST00000700021.1:c.958C>G ENSP00000514757.1:p.Arg320Gly
ENST00000700022.1:c.*342C>G ENSP00000514758.1:n.*342C>G
ENST00000700023.1:n.2161C>G
ENST00000700024.1:n.2395C>G
ENST00000700025.1:n.1772C>G
ENST00000700026.1:n.640C>G
ENST00000706954.1:c.1003C>G ENSP00000516674.1:p.Arg335Gly
ENST00000706955.1:c.*1038C>G ENSP00000516675.1:n.*1038C>G
ENST00000686459.1:c.*589C>G ENSP00000508909.1:n.*589C>G
ENST00000688158.1:c.*1114C>G ENSP00000509254.1:n.*1114C>G
ENST00000688308.1:c.1003C>G ENSP00000508752.1:p.Arg335Gly
ENST00000688922.1:c.924C>G
ENST00000693560.1:c.1522C>G ENSP00000509861.1:p.Arg508Gly
ENST00000371953.8:c.1003C>G MANE Select ENSP00000361021.3:p.Arg335Gly
ENST00000371953.7:c.1003C>G ENSP00000361021.3:p.Arg335Gly
ENST00000472832.2:c.430C>G ENSP00000483066.1:p.Arg144Gly
NM_000314.5:c.1003C>G NP_000305.3:p.Arg335Gly
NM_000314.6:c.1003C>G NP_000305.3:p.Arg335Gly
NM_001304717.2:c.1522C>G NP_001291646.2:p.Arg508Gly
NM_001304718.1:c.412C>G NP_001291647.1:p.Arg138Gly
XM_006717926.2:c.958C>G XP_006717989.1:p.Arg320Gly
XM_011539981.1:c.1003C>G XP_011538283.1:p.Arg335Gly
XM_011539982.1:c.907C>G XP_011538284.1:p.Arg303Gly
XR_945791.1:n.1573C>G
NM_000314.7:c.1003C>G NP_000305.3:p.Arg335Gly
NM_001304717.5:c.1522C>G NP_001291646.4:p.Arg508Gly
NM_001304718.2:c.412C>G NP_001291647.1:p.Arg138Gly
NM_000314.8:c.1003C>G MANE Select NP_000305.3:p.Arg335Gly