Canonical Allele Identifier: CA645369486
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 428249
ClinVar RCV Id: RCV000491609
dbSNP Id: rs1114167664

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957970_87957971delinsTG , CM000672.2:g.87957970_87957971delinsTG GRCh38
NC_000010.10:g.89717727_89717728delinsTG , CM000672.1:g.89717727_89717728delinsTG GRCh37
NC_000010.9:g.89707707_89707708delinsTG NCBI36
NG_007466.2:g.99532_99533delinsTG , LRG_311:g.99532_99533delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.752_753delinsTG ENSP00000514759.2:p.Gly251Val
ENST00000710265.1:c.752_753delinsTG ENSP00000518161.1:p.Gly251Val
ENST00000472832.3:c.752_753delinsTG ENSP00000483066.2:p.Gly251Val
ENST00000688158.2:n.1487_1488delinsTG
ENST00000688922.2:c.*582_*583delinsTG ENSP00000508742.2:n.*582_*583delinsTG
ENST00000700021.1:c.707_708delinsTG ENSP00000514757.1:p.Gly236Val
ENST00000700022.1:c.*91_*92delinsTG ENSP00000514758.1:n.*91_*92delinsTG
ENST00000700023.1:n.1910_1911delinsTG
ENST00000700024.1:n.2144_2145delinsTG
ENST00000700025.1:n.1521_1522delinsTG
ENST00000700026.1:n.389_390delinsTG
ENST00000700029.1:c.586_587delinsTG
ENST00000706954.1:c.752_753delinsTG ENSP00000516674.1:p.Gly251Val
ENST00000706955.1:c.*787_*788delinsTG ENSP00000516675.1:n.*787_*788delinsTG
ENST00000686459.1:c.*338_*339delinsTG ENSP00000508909.1:n.*338_*339delinsTG
ENST00000688158.1:c.*863_*864delinsTG ENSP00000509254.1:n.*863_*864delinsTG
ENST00000688308.1:c.752_753delinsTG ENSP00000508752.1:p.Gly251Val
ENST00000688922.1:c.673_674delinsTG
ENST00000693560.1:c.1271_1272delinsTG ENSP00000509861.1:p.Gly424Val
ENST00000371953.8:c.752_753delinsTG MANE Select ENSP00000361021.3:p.Gly251Val
ENST00000371953.7:c.752_753delinsTG ENSP00000361021.3:p.Gly251Val
ENST00000472832.2:c.179_180delinsTG ENSP00000483066.1:p.Gly60Val
NM_000314.5:c.752_753delinsTG NP_000305.3:p.Gly251Val
NM_000314.6:c.752_753delinsTG NP_000305.3:p.Gly251Val
NM_001304717.2:c.1271_1272delinsTG NP_001291646.2:p.Gly424Val
NM_001304718.1:c.161_162delinsTG NP_001291647.1:p.Gly54Val
XM_006717926.2:c.707_708delinsTG XP_006717989.1:p.Gly236Val
XM_011539981.1:c.752_753delinsTG XP_011538283.1:p.Gly251Val
XM_011539982.1:c.656_657delinsTG XP_011538284.1:p.Gly219Val
XR_945791.1:n.1322_1323delinsTG
NM_000314.7:c.752_753delinsTG NP_000305.3:p.Gly251Val
NM_001304717.5:c.1271_1272delinsTG NP_001291646.4:p.Gly424Val
NM_001304718.2:c.161_162delinsTG NP_001291647.1:p.Gly54Val
NM_000314.8:c.752_753delinsTG MANE Select NP_000305.3:p.Gly251Val