Canonical Allele Identifier: CA211247716
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs201259351

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87954231_87954232insT , CM000672.2:g.87954231_87954232insT GRCh38
NC_000010.10:g.89713988_89713989insT , CM000672.1:g.89713988_89713989insT GRCh37
NC_000010.9:g.89703968_89703969insT NCBI36
NG_007466.2:g.95793_95794insT , LRG_311:g.95793_95794insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.634+1972_634+1973insT ENSP00000514759.2:n.634+1972_634+1973insT
ENST00000710265.1:c.634+1972_634+1973insT ENSP00000518161.1:n.634+1972_634+1973insT
ENST00000472832.3:c.634+1972_634+1973insT ENSP00000483066.2:n.634+1972_634+1973insT
ENST00000688158.2:n.1369+1972_1369+1973insT
ENST00000688922.2:c.*464+1972_*464+1973insT ENSP00000508742.2:n.*464+1972_*464+1973insT
ENST00000700021.1:c.589+1972_589+1973insT ENSP00000514757.1:n.589+1972_589+1973insT
ENST00000700022.1:c.493-3622_493-3621insT ENSP00000514758.1:n.493-3622_493-3621insT
ENST00000700023.1:n.1792+1972_1792+1973insT
ENST00000700024.1:n.2026+1972_2026+1973insT
ENST00000700025.1:n.1403+1972_1403+1973insT
ENST00000700029.1:c.468+1972_468+1973insT
ENST00000706954.1:c.634+1972_634+1973insT ENSP00000516674.1:n.634+1972_634+1973insT
ENST00000706955.1:c.*669+1972_*669+1973insT ENSP00000516675.1:n.*669+1972_*669+1973insT
ENST00000686459.1:c.*220+1972_*220+1973insT ENSP00000508909.1:n.*220+1972_*220+1973insT
ENST00000688158.1:c.*745+1972_*745+1973insT ENSP00000509254.1:n.*745+1972_*745+1973insT
ENST00000688308.1:c.634+1972_634+1973insT ENSP00000508752.1:n.634+1972_634+1973insT
ENST00000688922.1:c.555+1972_555+1973insT
ENST00000693560.1:c.1153+1972_1153+1973insT ENSP00000509861.1:n.1153+1972_1153+1973insT
ENST00000371953.8:c.634+1972_634+1973insT MANE Select ENSP00000361021.3:n.634+1972_634+1973insT
ENST00000371953.7:c.634+1972_634+1973insT ENSP00000361021.3:n.634+1972_634+1973insT
ENST00000472832.2:c.61+1972_61+1973insT ENSP00000483066.1:n.61+1972_61+1973insT
NM_000314.5:c.634+1972_634+1973insT NP_000305.3:n.634+1972_634+1973insT
NM_000314.6:c.634+1972_634+1973insT NP_000305.3:n.634+1972_634+1973insT
NM_001304717.2:c.1153+1972_1153+1973insT NP_001291646.2:n.1153+1972_1153+1973insT
NM_001304718.1:c.43+1972_43+1973insT NP_001291647.1:n.43+1972_43+1973insT
XM_006717926.2:c.589+1972_589+1973insT XP_006717989.1:n.589+1972_589+1973insT
XM_011539981.1:c.634+1972_634+1973insT XP_011538283.1:n.634+1972_634+1973insT
XM_011539982.1:c.538+1972_538+1973insT XP_011538284.1:n.538+1972_538+1973insT
XR_945791.1:n.1205-3622_1205-3621insT
NM_000314.7:c.634+1972_634+1973insT NP_000305.3:n.634+1972_634+1973insT
NM_001304717.5:c.1153+1972_1153+1973insT NP_001291646.4:n.1153+1972_1153+1973insT
NM_001304718.2:c.43+1972_43+1973insT NP_001291647.1:n.43+1972_43+1973insT
NM_000314.8:c.634+1972_634+1973insT MANE Select NP_000305.3:n.634+1972_634+1973insT