Canonical Allele Identifier: CA891840069
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958003_87958004delinsTG , CM000672.2:g.87958003_87958004delinsTG GRCh38
NC_000010.10:g.89717760_89717761delinsTG , CM000672.1:g.89717760_89717761delinsTG GRCh37
NC_000010.9:g.89707740_89707741delinsTG NCBI36
NG_007466.2:g.99565_99566delinsTG , LRG_311:g.99565_99566delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.785_786delinsTG ENSP00000514759.2:p.Asn262Met
ENST00000710265.1:c.785_786delinsTG ENSP00000518161.1:p.Asn262Met
ENST00000472832.3:c.785_786delinsTG ENSP00000483066.2:p.Asn262Met
ENST00000688158.2:n.1520_1521delinsTG
ENST00000688922.2:c.*615_*616delinsTG ENSP00000508742.2:n.*615_*616delinsTG
ENST00000700021.1:c.740_741delinsTG ENSP00000514757.1:p.Asn247Met
ENST00000700022.1:c.*124_*125delinsTG ENSP00000514758.1:n.*124_*125delinsTG
ENST00000700023.1:n.1943_1944delinsTG
ENST00000700024.1:n.2177_2178delinsTG
ENST00000700025.1:n.1554_1555delinsTG
ENST00000700026.1:n.422_423delinsTG
ENST00000700029.1:c.619_620delinsTG
ENST00000706954.1:c.785_786delinsTG ENSP00000516674.1:p.Asn262Met
ENST00000706955.1:c.*820_*821delinsTG ENSP00000516675.1:n.*820_*821delinsTG
ENST00000686459.1:c.*371_*372delinsTG ENSP00000508909.1:n.*371_*372delinsTG
ENST00000688158.1:c.*896_*897delinsTG ENSP00000509254.1:n.*896_*897delinsTG
ENST00000688308.1:c.785_786delinsTG ENSP00000508752.1:p.Asn262Met
ENST00000688922.1:c.706_707delinsTG
ENST00000693560.1:c.1304_1305delinsTG ENSP00000509861.1:p.Asn435Met
ENST00000371953.8:c.785_786delinsTG MANE Select ENSP00000361021.3:p.Asn262Met
ENST00000371953.7:c.785_786delinsTG ENSP00000361021.3:p.Asn262Met
ENST00000472832.2:c.212_213delinsTG ENSP00000483066.1:p.Asn71Met
NM_000314.5:c.785_786delinsTG NP_000305.3:p.Asn262Met
NM_000314.6:c.785_786delinsTG NP_000305.3:p.Asn262Met
NM_001304717.2:c.1304_1305delinsTG NP_001291646.2:p.Asn435Met
NM_001304718.1:c.194_195delinsTG NP_001291647.1:p.Asn65Met
XM_006717926.2:c.740_741delinsTG XP_006717989.1:p.Asn247Met
XM_011539981.1:c.785_786delinsTG XP_011538283.1:p.Asn262Met
XM_011539982.1:c.689_690delinsTG XP_011538284.1:p.Asn230Met
XR_945791.1:n.1355_1356delinsTG
NM_000314.7:c.785_786delinsTG NP_000305.3:p.Asn262Met
NM_001304717.5:c.1304_1305delinsTG NP_001291646.4:p.Asn435Met
NM_001304718.2:c.194_195delinsTG NP_001291647.1:p.Asn65Met
NM_000314.8:c.785_786delinsTG MANE Select NP_000305.3:p.Asn262Met