Canonical Allele Identifier: CA1926188580
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957961_87957963delinsCTG , CM000672.2:g.87957961_87957963delinsCTG GRCh38
NC_000010.10:g.89717718_89717720delinsCTG , CM000672.1:g.89717718_89717720delinsCTG GRCh37
NC_000010.9:g.89707698_89707700delinsCTG NCBI36
NG_007466.2:g.99523_99525delinsCTG , LRG_311:g.99523_99525delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.743_745delinsCTG ENSP00000514759.2:p.Pro248=
ENST00000710265.1:c.743_745delinsCTG ENSP00000518161.1:p.Pro248=
ENST00000472832.3:c.743_745delinsCTG ENSP00000483066.2:p.Pro248=
ENST00000688158.2:n.1478_1480delinsCTG
ENST00000688922.2:c.*573_*575delinsCTG ENSP00000508742.2:n.*573_*575delinsCTG
ENST00000700021.1:c.698_700delinsCTG ENSP00000514757.1:p.Pro233=
ENST00000700022.1:c.*82_*84delinsCTG ENSP00000514758.1:n.*82_*84delinsCTG
ENST00000700023.1:n.1901_1903delinsCTG
ENST00000700024.1:n.2135_2137delinsCTG
ENST00000700025.1:n.1512_1514delinsCTG
ENST00000700026.1:n.380_382delinsCTG
ENST00000700029.1:c.577_579delinsCTG
ENST00000706954.1:c.743_745delinsCTG ENSP00000516674.1:p.Pro248=
ENST00000706955.1:c.*778_*780delinsCTG ENSP00000516675.1:n.*778_*780delinsCTG
ENST00000686459.1:c.*329_*331delinsCTG ENSP00000508909.1:n.*329_*331delinsCTG
ENST00000688158.1:c.*854_*856delinsCTG ENSP00000509254.1:n.*854_*856delinsCTG
ENST00000688308.1:c.743_745delinsCTG ENSP00000508752.1:p.Pro248=
ENST00000688922.1:c.664_666delinsCTG
ENST00000693560.1:c.1262_1264delinsCTG ENSP00000509861.1:p.Pro421=
ENST00000371953.8:c.743_745delinsCTG MANE Select ENSP00000361021.3:p.Pro248=
ENST00000371953.7:c.743_745delinsCTG ENSP00000361021.3:p.Pro248=
ENST00000472832.2:c.170_172delinsCTG ENSP00000483066.1:p.Pro57=
NM_000314.5:c.743_745delinsCTG NP_000305.3:p.Pro248=
NM_000314.6:c.743_745delinsCTG NP_000305.3:p.Pro248=
NM_001304717.2:c.1262_1264delinsCTG NP_001291646.2:p.Pro421=
NM_001304718.1:c.152_154delinsCTG NP_001291647.1:p.Pro51=
XM_006717926.2:c.698_700delinsCTG XP_006717989.1:p.Pro233=
XM_011539981.1:c.743_745delinsCTG XP_011538283.1:p.Pro248=
XM_011539982.1:c.647_649delinsCTG XP_011538284.1:p.Pro216=
XR_945791.1:n.1313_1315delinsCTG
NM_000314.7:c.743_745delinsCTG NP_000305.3:p.Pro248=
NM_001304717.5:c.1262_1264delinsCTG NP_001291646.4:p.Pro421=
NM_001304718.2:c.152_154delinsCTG NP_001291647.1:p.Pro51=
NM_000314.8:c.743_745delinsCTG MANE Select NP_000305.3:p.Pro248=