Canonical Allele Identifier: CA891840132
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958017_87958019delinsTGT , CM000672.2:g.87958017_87958019delinsTGT GRCh38
NC_000010.10:g.89717774_89717776delinsTGT , CM000672.1:g.89717774_89717776delinsTGT GRCh37
NC_000010.9:g.89707754_89707756delinsTGT NCBI36
NG_007466.2:g.99579_99581delinsTGT , LRG_311:g.99579_99581delinsTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.799_801delinsTGT ENSP00000514759.2:p.Lys267Cys
ENST00000710265.1:c.799_801delinsTGT ENSP00000518161.1:p.Lys267Cys
ENST00000472832.3:c.799_801delinsTGT ENSP00000483066.2:p.Lys267Cys
ENST00000688158.2:n.1534_1536delinsTGT
ENST00000688922.2:c.*629_*631delinsTGT ENSP00000508742.2:n.*629_*631delinsTGT
ENST00000700021.1:c.754_756delinsTGT ENSP00000514757.1:p.Lys252Cys
ENST00000700022.1:c.*138_*140delinsTGT ENSP00000514758.1:n.*138_*140delinsTGT
ENST00000700023.1:n.1957_1959delinsTGT
ENST00000700024.1:n.2191_2193delinsTGT
ENST00000700025.1:n.1568_1570delinsTGT
ENST00000700026.1:n.436_438delinsTGT
ENST00000700029.1:c.633_635delinsTGT
ENST00000706954.1:c.799_801delinsTGT ENSP00000516674.1:p.Lys267Cys
ENST00000706955.1:c.*834_*836delinsTGT ENSP00000516675.1:n.*834_*836delinsTGT
ENST00000686459.1:c.*385_*387delinsTGT ENSP00000508909.1:n.*385_*387delinsTGT
ENST00000688158.1:c.*910_*912delinsTGT ENSP00000509254.1:n.*910_*912delinsTGT
ENST00000688308.1:c.799_801delinsTGT ENSP00000508752.1:p.Lys267Cys
ENST00000688922.1:c.720_722delinsTGT
ENST00000693560.1:c.1318_1320delinsTGT ENSP00000509861.1:p.Lys440Cys
ENST00000371953.8:c.799_801delinsTGT MANE Select ENSP00000361021.3:p.Lys267Cys
ENST00000371953.7:c.799_801delinsTGT ENSP00000361021.3:p.Lys267Cys
ENST00000472832.2:c.226_228delinsTGT ENSP00000483066.1:p.Lys76Cys
NM_000314.5:c.799_801delinsTGT NP_000305.3:p.Lys267Cys
NM_000314.6:c.799_801delinsTGT NP_000305.3:p.Lys267Cys
NM_001304717.2:c.1318_1320delinsTGT NP_001291646.2:p.Lys440Cys
NM_001304718.1:c.208_210delinsTGT NP_001291647.1:p.Lys70Cys
XM_006717926.2:c.754_756delinsTGT XP_006717989.1:p.Lys252Cys
XM_011539981.1:c.799_801delinsTGT XP_011538283.1:p.Lys267Cys
XM_011539982.1:c.703_705delinsTGT XP_011538284.1:p.Lys235Cys
XR_945791.1:n.1369_1371delinsTGT
NM_000314.7:c.799_801delinsTGT NP_000305.3:p.Lys267Cys
NM_001304717.5:c.1318_1320delinsTGT NP_001291646.4:p.Lys440Cys
NM_001304718.2:c.208_210delinsTGT NP_001291647.1:p.Lys70Cys
NM_000314.8:c.799_801delinsTGT MANE Select NP_000305.3:p.Lys267Cys