Canonical Allele Identifier: CA377484772
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957862T>G , CM000672.2:g.87957862T>G GRCh38
NC_000010.10:g.89717619T>G , CM000672.1:g.89717619T>G GRCh37
NC_000010.9:g.89707599T>G NCBI36
NG_007466.2:g.99424T>G , LRG_311:g.99424T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.644T>G ENSP00000514759.2:p.Phe215Cys
ENST00000710265.1:c.644T>G ENSP00000518161.1:p.Phe215Cys
ENST00000472832.3:c.644T>G ENSP00000483066.2:p.Phe215Cys
ENST00000688158.2:n.1379T>G
ENST00000688922.2:c.*474T>G ENSP00000508742.2:n.*474T>G
ENST00000700021.1:c.599T>G ENSP00000514757.1:p.Phe200Cys
ENST00000700022.1:c.502T>G ENSP00000514758.1:p.Leu168Val
ENST00000700023.1:n.1802T>G
ENST00000700024.1:n.2036T>G
ENST00000700025.1:n.1413T>G
ENST00000700026.1:n.281T>G
ENST00000700029.1:c.478T>G
ENST00000706954.1:c.644T>G ENSP00000516674.1:p.Phe215Cys
ENST00000706955.1:c.*679T>G ENSP00000516675.1:n.*679T>G
ENST00000686459.1:c.*230T>G ENSP00000508909.1:n.*230T>G
ENST00000688158.1:c.*755T>G ENSP00000509254.1:n.*755T>G
ENST00000688308.1:c.644T>G ENSP00000508752.1:p.Phe215Cys
ENST00000688922.1:c.565T>G
ENST00000693560.1:c.1163T>G ENSP00000509861.1:p.Phe388Cys
ENST00000371953.8:c.644T>G MANE Select ENSP00000361021.3:p.Phe215Cys
ENST00000371953.7:c.644T>G ENSP00000361021.3:p.Phe215Cys
ENST00000472832.2:c.71T>G ENSP00000483066.1:p.Phe24Cys
NM_000314.5:c.644T>G NP_000305.3:p.Phe215Cys
NM_000314.6:c.644T>G NP_000305.3:p.Phe215Cys
NM_001304717.2:c.1163T>G NP_001291646.2:p.Phe388Cys
NM_001304718.1:c.53T>G NP_001291647.1:p.Phe18Cys
XM_006717926.2:c.599T>G XP_006717989.1:p.Phe200Cys
XM_011539981.1:c.644T>G XP_011538283.1:p.Phe215Cys
XM_011539982.1:c.548T>G XP_011538284.1:p.Phe183Cys
XR_945791.1:n.1214T>G
NM_000314.7:c.644T>G NP_000305.3:p.Phe215Cys
NM_001304717.5:c.1163T>G NP_001291646.4:p.Phe388Cys
NM_001304718.2:c.53T>G NP_001291647.1:p.Phe18Cys
NM_000314.8:c.644T>G MANE Select NP_000305.3:p.Phe215Cys