Canonical Allele Identifier: CA891840138
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958017_87958019delinsTTT , CM000672.2:g.87958017_87958019delinsTTT GRCh38
NC_000010.10:g.89717774_89717776delinsTTT , CM000672.1:g.89717774_89717776delinsTTT GRCh37
NC_000010.9:g.89707754_89707756delinsTTT NCBI36
NG_007466.2:g.99579_99581delinsTTT , LRG_311:g.99579_99581delinsTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.799_801delinsTTT ENSP00000514759.2:p.Lys267Phe
ENST00000710265.1:c.799_801delinsTTT ENSP00000518161.1:p.Lys267Phe
ENST00000472832.3:c.799_801delinsTTT ENSP00000483066.2:p.Lys267Phe
ENST00000688158.2:n.1534_1536delinsTTT
ENST00000688922.2:c.*629_*631delinsTTT ENSP00000508742.2:n.*629_*631delinsTTT
ENST00000700021.1:c.754_756delinsTTT ENSP00000514757.1:p.Lys252Phe
ENST00000700022.1:c.*138_*140delinsTTT ENSP00000514758.1:n.*138_*140delinsTTT
ENST00000700023.1:n.1957_1959delinsTTT
ENST00000700024.1:n.2191_2193delinsTTT
ENST00000700025.1:n.1568_1570delinsTTT
ENST00000700026.1:n.436_438delinsTTT
ENST00000700029.1:c.633_635delinsTTT
ENST00000706954.1:c.799_801delinsTTT ENSP00000516674.1:p.Lys267Phe
ENST00000706955.1:c.*834_*836delinsTTT ENSP00000516675.1:n.*834_*836delinsTTT
ENST00000686459.1:c.*385_*387delinsTTT ENSP00000508909.1:n.*385_*387delinsTTT
ENST00000688158.1:c.*910_*912delinsTTT ENSP00000509254.1:n.*910_*912delinsTTT
ENST00000688308.1:c.799_801delinsTTT ENSP00000508752.1:p.Lys267Phe
ENST00000688922.1:c.720_722delinsTTT
ENST00000693560.1:c.1318_1320delinsTTT ENSP00000509861.1:p.Lys440Phe
ENST00000371953.8:c.799_801delinsTTT MANE Select ENSP00000361021.3:p.Lys267Phe
ENST00000371953.7:c.799_801delinsTTT ENSP00000361021.3:p.Lys267Phe
ENST00000472832.2:c.226_228delinsTTT ENSP00000483066.1:p.Lys76Phe
NM_000314.5:c.799_801delinsTTT NP_000305.3:p.Lys267Phe
NM_000314.6:c.799_801delinsTTT NP_000305.3:p.Lys267Phe
NM_001304717.2:c.1318_1320delinsTTT NP_001291646.2:p.Lys440Phe
NM_001304718.1:c.208_210delinsTTT NP_001291647.1:p.Lys70Phe
XM_006717926.2:c.754_756delinsTTT XP_006717989.1:p.Lys252Phe
XM_011539981.1:c.799_801delinsTTT XP_011538283.1:p.Lys267Phe
XM_011539982.1:c.703_705delinsTTT XP_011538284.1:p.Lys235Phe
XR_945791.1:n.1369_1371delinsTTT
NM_000314.7:c.799_801delinsTTT NP_000305.3:p.Lys267Phe
NM_001304717.5:c.1318_1320delinsTTT NP_001291646.4:p.Lys440Phe
NM_001304718.2:c.208_210delinsTTT NP_001291647.1:p.Lys70Phe
NM_000314.8:c.799_801delinsTTT MANE Select NP_000305.3:p.Lys267Phe