Canonical Allele Identifier: CA2722449296
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132284067

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961203A>G , CM000672.2:g.87961203A>G GRCh38
NC_000010.10:g.89720960A>G , CM000672.1:g.89720960A>G GRCh37
NC_000010.9:g.89710940A>G NCBI36
NG_007466.2:g.102765A>G , LRG_311:g.102765A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1119+85A>G ENSP00000514759.2:n.1119+85A>G
ENST00000710265.1:c.1026+85A>G ENSP00000518161.1:n.1026+85A>G
ENST00000472832.3:c.*76A>G ENSP00000483066.2:n.*76A>G
ENST00000688158.2:n.1761+85A>G
ENST00000688922.2:c.*856+85A>G ENSP00000508742.2:n.*856+85A>G
ENST00000700021.1:c.981+85A>G ENSP00000514757.1:n.981+85A>G
ENST00000700022.1:c.*365+85A>G ENSP00000514758.1:n.*365+85A>G
ENST00000700023.1:n.2184+85A>G
ENST00000700024.1:n.2418+85A>G
ENST00000700025.1:n.1880A>G
ENST00000700026.1:n.748A>G
ENST00000706954.1:c.1026+85A>G ENSP00000516674.1:n.1026+85A>G
ENST00000706955.1:c.*1061+85A>G ENSP00000516675.1:n.*1061+85A>G
ENST00000686459.1:c.*612+85A>G ENSP00000508909.1:n.*612+85A>G
ENST00000688158.1:c.*1137+85A>G ENSP00000509254.1:n.*1137+85A>G
ENST00000688308.1:c.1026+85A>G ENSP00000508752.1:n.1026+85A>G
ENST00000688922.1:c.947+85A>G
ENST00000693560.1:c.1545+85A>G ENSP00000509861.1:n.1545+85A>G
ENST00000371953.8:c.1026+85A>G MANE Select ENSP00000361021.3:n.1026+85A>G
ENST00000371953.7:c.1026+85A>G ENSP00000361021.3:n.1026+85A>G
ENST00000472832.2:c.538A>G ENSP00000483066.1:n.538A>G
NM_000314.5:c.1026+85A>G NP_000305.3:n.1026+85A>G
NM_000314.6:c.1026+85A>G NP_000305.3:n.1026+85A>G
NM_001304717.2:c.1545+85A>G NP_001291646.2:n.1545+85A>G
NM_001304718.1:c.435+85A>G NP_001291647.1:n.435+85A>G
XM_006717926.2:c.981+85A>G XP_006717989.1:n.981+85A>G
XM_011539981.1:c.1026+85A>G XP_011538283.1:n.1026+85A>G
XM_011539982.1:c.930+85A>G XP_011538284.1:n.930+85A>G
XR_945791.1:n.1596+85A>G
NM_000314.7:c.1026+85A>G NP_000305.3:n.1026+85A>G
NM_001304717.5:c.1545+85A>G NP_001291646.4:n.1545+85A>G
NM_001304718.2:c.435+85A>G NP_001291647.1:n.435+85A>G
NM_000314.8:c.1026+85A>G MANE Select NP_000305.3:n.1026+85A>G