Canonical Allele Identifier: CA891837224
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965329_87965331delinsGGT , CM000672.2:g.87965329_87965331delinsGGT GRCh38
NC_000010.10:g.89725086_89725088delinsGGT , CM000672.1:g.89725086_89725088delinsGGT GRCh37
NC_000010.9:g.89715066_89715068delinsGGT NCBI36
NG_007466.2:g.106891_106893delinsGGT , LRG_311:g.106891_106893delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1162_1164delinsGGT ENSP00000514759.2:p.Pro388Gly
ENST00000710265.1:c.*98_*100delinsGGT ENSP00000518161.1:n.*98_*100delinsGGT
ENST00000688158.2:n.1804_1806delinsGGT
ENST00000688922.2:c.*899_*901delinsGGT ENSP00000508742.2:n.*899_*901delinsGGT
ENST00000700021.1:c.1024_1026delinsGGT ENSP00000514757.1:p.Pro342Gly
ENST00000700022.1:c.*408_*410delinsGGT ENSP00000514758.1:n.*408_*410delinsGGT
ENST00000700023.1:n.2227_2229delinsGGT
ENST00000700024.1:n.2461_2463delinsGGT
ENST00000706954.1:c.1069_1071delinsGGT ENSP00000516674.1:p.Pro357Gly
ENST00000706955.1:c.*1104_*1106delinsGGT ENSP00000516675.1:n.*1104_*1106delinsGGT
ENST00000686459.1:c.*655_*657delinsGGT ENSP00000508909.1:n.*655_*657delinsGGT
ENST00000688158.1:c.*1180_*1182delinsGGT ENSP00000509254.1:n.*1180_*1182delinsGGT
ENST00000688308.1:c.1069_1071delinsGGT ENSP00000508752.1:p.Pro357Gly
ENST00000688922.1:c.990_992delinsGGT
ENST00000693560.1:c.1588_1590delinsGGT ENSP00000509861.1:p.Pro530Gly
ENST00000371953.8:c.1069_1071delinsGGT MANE Select ENSP00000361021.3:p.Pro357Gly
ENST00000371953.7:c.1069_1071delinsGGT ENSP00000361021.3:p.Pro357Gly
NM_000314.5:c.1069_1071delinsGGT NP_000305.3:p.Pro357Gly
NM_000314.6:c.1069_1071delinsGGT NP_000305.3:p.Pro357Gly
NM_001304717.2:c.1588_1590delinsGGT NP_001291646.2:p.Pro530Gly
NM_001304718.1:c.478_480delinsGGT NP_001291647.1:p.Pro160Gly
XM_006717926.2:c.1024_1026delinsGGT XP_006717989.1:p.Pro342Gly
XM_011539982.1:c.973_975delinsGGT XP_011538284.1:p.Pro325Gly
XR_945791.1:n.1639_1641delinsGGT
NM_000314.7:c.1069_1071delinsGGT NP_000305.3:p.Pro357Gly
NM_001304717.5:c.1588_1590delinsGGT NP_001291646.4:p.Pro530Gly
NM_001304718.2:c.478_480delinsGGT NP_001291647.1:p.Pro160Gly
NM_000314.8:c.1069_1071delinsGGT MANE Select NP_000305.3:p.Pro357Gly