Canonical Allele Identifier: CA377784472
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 1456749
ClinVar RCV Id: RCV001946963
dbSNP Id: rs786204854
COSMIC: COSM5311

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87894051G>T , CM000672.2:g.87894051G>T GRCh38
NC_000010.10:g.89653808G>T , CM000672.1:g.89653808G>T GRCh37
NC_000010.9:g.89643788G>T NCBI36
NG_007466.2:g.35613G>T , LRG_311:g.35613G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.106G>T ENSP00000514759.2:p.Gly36Ter
ENST00000710265.1:c.106G>T ENSP00000518161.1:p.Gly36Ter
ENST00000472832.3:c.106G>T ENSP00000483066.2:p.Gly36Ter
ENST00000688158.2:n.899+13613G>T
ENST00000688922.2:c.106G>T ENSP00000508742.2:p.Gly36Ter
ENST00000700021.1:c.106G>T ENSP00000514757.1:p.Gly36Ter
ENST00000700022.1:c.106G>T ENSP00000514758.1:p.Gly36Ter
ENST00000706954.1:c.106G>T ENSP00000516674.1:p.Gly36Ter
ENST00000706955.1:c.*141G>T ENSP00000516675.1:n.*141G>T
ENST00000686459.1:c.106G>T ENSP00000508909.1:p.Gly36Ter
ENST00000688158.1:c.*275+13613G>T ENSP00000509254.1:n.*275+13613G>T
ENST00000688308.1:c.106G>T ENSP00000508752.1:p.Gly36Ter
ENST00000693560.1:c.625G>T ENSP00000509861.1:p.Gly209Ter
ENST00000371953.8:c.106G>T MANE Select ENSP00000361021.3:p.Gly36Ter
ENST00000371953.7:c.106G>T ENSP00000361021.3:p.Gly36Ter
ENST00000462694.1:n.108G>T
ENST00000610634.1:c.4G>T ENSP00000477517.1:p.Gly2Ter
NM_000314.5:c.106G>T NP_000305.3:p.Gly36Ter
NM_000314.6:c.106G>T NP_000305.3:p.Gly36Ter
NM_001304717.2:c.625G>T NP_001291646.2:p.Gly209Ter
NM_001304718.1:c.-600G>T NP_001291647.1:n.-600G>T
XM_006717926.2:c.106G>T XP_006717989.1:p.Gly36Ter
XM_011539981.1:c.106G>T XP_011538283.1:p.Gly36Ter
XM_011539982.1:c.68+13613G>T XP_011538284.1:n.68+13613G>T
XR_945789.1:n.818G>T
XR_945790.1:n.818G>T
XR_945791.1:n.818G>T
NM_000314.7:c.106G>T NP_000305.3:p.Gly36Ter
NM_001304717.5:c.625G>T NP_001291646.4:p.Gly209Ter
NM_001304718.2:c.-600G>T NP_001291647.1:n.-600G>T
NM_000314.8:c.106G>T MANE Select NP_000305.3:p.Gly36Ter