Canonical Allele Identifier: CA658683584
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 492339
ClinVar RCV Id: RCV000583097
dbSNP Id: rs1554825222

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957959_87957960dup , CM000672.2:g.87957959_87957960dup GRCh38
NC_000010.10:g.89717716_89717717dup , CM000672.1:g.89717716_89717717dup GRCh37
NC_000010.9:g.89707696_89707697dup NCBI36
NG_007466.2:g.99521_99522dup , LRG_311:g.99521_99522dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.741_742dup ENSP00000514759.2:p.Pro248HisfsTer9
ENST00000710265.1:c.741_742dup ENSP00000518161.1:p.Pro248HisfsTer9
ENST00000472832.3:c.741_742dup ENSP00000483066.2:p.Pro248HisfsTer9
ENST00000688158.2:n.1476_1477dup
ENST00000688922.2:c.*571_*572dup ENSP00000508742.2:n.*571_*572dup
ENST00000700021.1:c.696_697dup ENSP00000514757.1:p.Pro233HisfsTer9
ENST00000700022.1:c.*80_*81dup ENSP00000514758.1:n.*80_*81dup
ENST00000700023.1:n.1899_1900dup
ENST00000700024.1:n.2133_2134dup
ENST00000700025.1:n.1510_1511dup
ENST00000700026.1:n.378_379dup
ENST00000700029.1:c.575_576dup
ENST00000706954.1:c.741_742dup ENSP00000516674.1:p.Pro248HisfsTer9
ENST00000706955.1:c.*776_*777dup ENSP00000516675.1:n.*776_*777dup
ENST00000686459.1:c.*327_*328dup ENSP00000508909.1:n.*327_*328dup
ENST00000688158.1:c.*852_*853dup ENSP00000509254.1:n.*852_*853dup
ENST00000688308.1:c.741_742dup ENSP00000508752.1:p.Pro248HisfsTer9
ENST00000688922.1:c.662_663dup
ENST00000693560.1:c.1260_1261dup ENSP00000509861.1:p.Pro421HisfsTer9
ENST00000371953.8:c.741_742dup MANE Select ENSP00000361021.3:p.Pro248HisfsTer9
ENST00000371953.7:c.741_742dup ENSP00000361021.3:p.Pro248HisfsTer9
ENST00000472832.2:c.168_169dup ENSP00000483066.1:p.Pro57HisfsTer9
NM_000314.5:c.741_742dup NP_000305.3:p.Pro248HisfsTer9
NM_000314.6:c.741_742dup NP_000305.3:p.Pro248HisfsTer9
NM_001304717.2:c.1260_1261dup NP_001291646.2:p.Pro421HisfsTer9
NM_001304718.1:c.150_151dup NP_001291647.1:p.Pro51HisfsTer9
XM_006717926.2:c.696_697dup XP_006717989.1:p.Pro233HisfsTer9
XM_011539981.1:c.741_742dup XP_011538283.1:p.Pro248HisfsTer9
XM_011539982.1:c.645_646dup XP_011538284.1:p.Pro216HisfsTer9
XR_945791.1:n.1311_1312dup
NM_000314.7:c.741_742dup NP_000305.3:p.Pro248HisfsTer9
NM_001304717.5:c.1260_1261dup NP_001291646.4:p.Pro421HisfsTer9
NM_001304718.2:c.150_151dup NP_001291647.1:p.Pro51HisfsTer9
NM_000314.8:c.741_742dup MANE Select NP_000305.3:p.Pro248HisfsTer9