Canonical Allele Identifier: CA377781944
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 536556
dbSNP Id: rs587782187
COSMIC: COSM921056

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87864517T>G , CM000672.2:g.87864517T>G GRCh38
NC_000010.10:g.89624274T>G , CM000672.1:g.89624274T>G GRCh37
NC_000010.9:g.89614254T>G NCBI36
NG_007466.2:g.6079T>G , LRG_311:g.6079T>G
NG_033079.1:g.3921A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.48T>G ENSP00000514759.2:p.Tyr16Ter
ENST00000710265.1:c.48T>G ENSP00000518161.1:p.Tyr16Ter
ENST00000472832.3:c.48T>G ENSP00000483066.2:p.Tyr16Ter
ENST00000688922.2:c.48T>G ENSP00000508742.2:p.Tyr16Ter
ENST00000700021.1:c.48T>G ENSP00000514757.1:p.Tyr16Ter
ENST00000700022.1:c.48T>G ENSP00000514758.1:p.Tyr16Ter
ENST00000706954.1:c.48T>G ENSP00000516674.1:p.Tyr16Ter
ENST00000706955.1:c.48T>G ENSP00000516675.1:p.Tyr16Ter
ENST00000686459.1:c.48T>G ENSP00000508909.1:p.Tyr16Ter
ENST00000688158.1:c.48T>G ENSP00000509254.1:p.Tyr16Ter
ENST00000688308.1:c.48T>G ENSP00000508752.1:p.Tyr16Ter
ENST00000693560.1:c.567T>G ENSP00000509861.1:p.Tyr189Ter
ENST00000371953.8:c.48T>G MANE Select ENSP00000361021.3:p.Tyr16Ter
ENST00000371953.7:c.48T>G ENSP00000361021.3:p.Tyr16Ter
ENST00000462694.1:n.50T>G
ENST00000487939.1:n.69T>G
ENST00000610634.1:c.-55T>G ENSP00000477517.1:n.-55T>G
ENST00000618586.1:n.17T>G
NM_000314.5:c.48T>G NP_000305.3:p.Tyr16Ter
NM_000314.6:c.48T>G NP_000305.3:p.Tyr16Ter
NM_001304717.2:c.567T>G NP_001291646.2:p.Tyr189Ter
NM_001304718.1:c.-658T>G NP_001291647.1:n.-658T>G
XM_006717926.2:c.48T>G XP_006717989.1:p.Tyr16Ter
XM_011539981.1:c.48T>G XP_011538283.1:p.Tyr16Ter
XR_945789.1:n.760T>G
XR_945790.1:n.760T>G
XR_945791.1:n.760T>G
NM_000314.7:c.48T>G NP_000305.3:p.Tyr16Ter
NM_001304717.5:c.567T>G NP_001291646.4:p.Tyr189Ter
NM_001304718.2:c.-658T>G NP_001291647.1:n.-658T>G
NM_000314.8:c.48T>G MANE Select NP_000305.3:p.Tyr16Ter