Canonical Allele Identifier: CA891840971
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958015_87958016delinsTG , CM000672.2:g.87958015_87958016delinsTG GRCh38
NC_000010.10:g.89717772_89717773delinsTG , CM000672.1:g.89717772_89717773delinsTG GRCh37
NC_000010.9:g.89707752_89707753delinsTG NCBI36
NG_007466.2:g.99577_99578delinsTG , LRG_311:g.99577_99578delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.797_798delinsTG ENSP00000514759.2:p.Lys266Met
ENST00000710265.1:c.797_798delinsTG ENSP00000518161.1:p.Lys266Met
ENST00000472832.3:c.797_798delinsTG ENSP00000483066.2:p.Lys266Met
ENST00000688158.2:n.1532_1533delinsTG
ENST00000688922.2:c.*627_*628delinsTG ENSP00000508742.2:n.*627_*628delinsTG
ENST00000700021.1:c.752_753delinsTG ENSP00000514757.1:p.Lys251Met
ENST00000700022.1:c.*136_*137delinsTG ENSP00000514758.1:n.*136_*137delinsTG
ENST00000700023.1:n.1955_1956delinsTG
ENST00000700024.1:n.2189_2190delinsTG
ENST00000700025.1:n.1566_1567delinsTG
ENST00000700026.1:n.434_435delinsTG
ENST00000700029.1:c.631_632delinsTG
ENST00000706954.1:c.797_798delinsTG ENSP00000516674.1:p.Lys266Met
ENST00000706955.1:c.*832_*833delinsTG ENSP00000516675.1:n.*832_*833delinsTG
ENST00000686459.1:c.*383_*384delinsTG ENSP00000508909.1:n.*383_*384delinsTG
ENST00000688158.1:c.*908_*909delinsTG ENSP00000509254.1:n.*908_*909delinsTG
ENST00000688308.1:c.797_798delinsTG ENSP00000508752.1:p.Lys266Met
ENST00000688922.1:c.718_719delinsTG
ENST00000693560.1:c.1316_1317delinsTG ENSP00000509861.1:p.Lys439Met
ENST00000371953.8:c.797_798delinsTG MANE Select ENSP00000361021.3:p.Lys266Met
ENST00000371953.7:c.797_798delinsTG ENSP00000361021.3:p.Lys266Met
ENST00000472832.2:c.224_225delinsTG ENSP00000483066.1:p.Lys75Met
NM_000314.5:c.797_798delinsTG NP_000305.3:p.Lys266Met
NM_000314.6:c.797_798delinsTG NP_000305.3:p.Lys266Met
NM_001304717.2:c.1316_1317delinsTG NP_001291646.2:p.Lys439Met
NM_001304718.1:c.206_207delinsTG NP_001291647.1:p.Lys69Met
XM_006717926.2:c.752_753delinsTG XP_006717989.1:p.Lys251Met
XM_011539981.1:c.797_798delinsTG XP_011538283.1:p.Lys266Met
XM_011539982.1:c.701_702delinsTG XP_011538284.1:p.Lys234Met
XR_945791.1:n.1367_1368delinsTG
NM_000314.7:c.797_798delinsTG NP_000305.3:p.Lys266Met
NM_001304717.5:c.1316_1317delinsTG NP_001291646.4:p.Lys439Met
NM_001304718.2:c.206_207delinsTG NP_001291647.1:p.Lys69Met
NM_000314.8:c.797_798delinsTG MANE Select NP_000305.3:p.Lys266Met