Canonical Allele Identifier: CA669551177
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs879617800

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87954233_87954234dup , CM000672.2:g.87954233_87954234dup GRCh38
NC_000010.10:g.89713990_89713991dup , CM000672.1:g.89713990_89713991dup GRCh37
NC_000010.9:g.89703970_89703971dup NCBI36
NG_007466.2:g.95795_95796dup , LRG_311:g.95795_95796dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.634+1974_634+1975dup ENSP00000514759.2:n.634+1974_634+1975dup
ENST00000710265.1:c.634+1974_634+1975dup ENSP00000518161.1:n.634+1974_634+1975dup
ENST00000472832.3:c.634+1974_634+1975dup ENSP00000483066.2:n.634+1974_634+1975dup
ENST00000688158.2:n.1369+1974_1369+1975dup
ENST00000688922.2:c.*464+1974_*464+1975dup ENSP00000508742.2:n.*464+1974_*464+1975dup
ENST00000700021.1:c.589+1974_589+1975dup ENSP00000514757.1:n.589+1974_589+1975dup
ENST00000700022.1:c.493-3620_493-3619dup ENSP00000514758.1:n.493-3620_493-3619dup
ENST00000700023.1:n.1792+1974_1792+1975dup
ENST00000700024.1:n.2026+1974_2026+1975dup
ENST00000700025.1:n.1403+1974_1403+1975dup
ENST00000700029.1:c.468+1974_468+1975dup
ENST00000706954.1:c.634+1974_634+1975dup ENSP00000516674.1:n.634+1974_634+1975dup
ENST00000706955.1:c.*669+1974_*669+1975dup ENSP00000516675.1:n.*669+1974_*669+1975dup
ENST00000686459.1:c.*220+1974_*220+1975dup ENSP00000508909.1:n.*220+1974_*220+1975dup
ENST00000688158.1:c.*745+1974_*745+1975dup ENSP00000509254.1:n.*745+1974_*745+1975dup
ENST00000688308.1:c.634+1974_634+1975dup ENSP00000508752.1:n.634+1974_634+1975dup
ENST00000688922.1:c.555+1974_555+1975dup
ENST00000693560.1:c.1153+1974_1153+1975dup ENSP00000509861.1:n.1153+1974_1153+1975dup
ENST00000371953.8:c.634+1974_634+1975dup MANE Select ENSP00000361021.3:n.634+1974_634+1975dup
ENST00000371953.7:c.634+1974_634+1975dup ENSP00000361021.3:n.634+1974_634+1975dup
ENST00000472832.2:c.61+1974_61+1975dup ENSP00000483066.1:n.61+1974_61+1975dup
NM_000314.5:c.634+1974_634+1975dup NP_000305.3:n.634+1974_634+1975dup
NM_000314.6:c.634+1974_634+1975dup NP_000305.3:n.634+1974_634+1975dup
NM_001304717.2:c.1153+1974_1153+1975dup NP_001291646.2:n.1153+1974_1153+1975dup
NM_001304718.1:c.43+1974_43+1975dup NP_001291647.1:n.43+1974_43+1975dup
XM_006717926.2:c.589+1974_589+1975dup XP_006717989.1:n.589+1974_589+1975dup
XM_011539981.1:c.634+1974_634+1975dup XP_011538283.1:n.634+1974_634+1975dup
XM_011539982.1:c.538+1974_538+1975dup XP_011538284.1:n.538+1974_538+1975dup
XR_945791.1:n.1205-3620_1205-3619dup
NM_000314.7:c.634+1974_634+1975dup NP_000305.3:n.634+1974_634+1975dup
NM_001304717.5:c.1153+1974_1153+1975dup NP_001291646.4:n.1153+1974_1153+1975dup
NM_001304718.2:c.43+1974_43+1975dup NP_001291647.1:n.43+1974_43+1975dup
NM_000314.8:c.634+1974_634+1975dup MANE Select NP_000305.3:n.634+1974_634+1975dup