Canonical Allele Identifier: CA377486127
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs1085308040

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961096G>C , CM000672.2:g.87961096G>C GRCh38
NC_000010.10:g.89720853G>C , CM000672.1:g.89720853G>C GRCh37
NC_000010.9:g.89710833G>C NCBI36
NG_007466.2:g.102658G>C , LRG_311:g.102658G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.1097G>C ENSP00000514759.2:p.Arg366Pro
ENST00000710265.1:c.1004G>C ENSP00000518161.1:p.Arg335Pro
ENST00000472832.3:c.1004G>C ENSP00000483066.2:p.Arg335Pro
ENST00000688158.2:n.1739G>C
ENST00000688922.2:c.*834G>C ENSP00000508742.2:n.*834G>C
ENST00000700021.1:c.959G>C ENSP00000514757.1:p.Arg320Pro
ENST00000700022.1:c.*343G>C ENSP00000514758.1:n.*343G>C
ENST00000700023.1:n.2162G>C
ENST00000700024.1:n.2396G>C
ENST00000700025.1:n.1773G>C
ENST00000700026.1:n.641G>C
ENST00000706954.1:c.1004G>C ENSP00000516674.1:p.Arg335Pro
ENST00000706955.1:c.*1039G>C ENSP00000516675.1:n.*1039G>C
ENST00000686459.1:c.*590G>C ENSP00000508909.1:n.*590G>C
ENST00000688158.1:c.*1115G>C ENSP00000509254.1:n.*1115G>C
ENST00000688308.1:c.1004G>C ENSP00000508752.1:p.Arg335Pro
ENST00000688922.1:c.925G>C
ENST00000693560.1:c.1523G>C ENSP00000509861.1:p.Arg508Pro
ENST00000371953.8:c.1004G>C MANE Select ENSP00000361021.3:p.Arg335Pro
ENST00000371953.7:c.1004G>C ENSP00000361021.3:p.Arg335Pro
ENST00000472832.2:c.431G>C ENSP00000483066.1:p.Arg144Pro
NM_000314.5:c.1004G>C NP_000305.3:p.Arg335Pro
NM_000314.6:c.1004G>C NP_000305.3:p.Arg335Pro
NM_001304717.2:c.1523G>C NP_001291646.2:p.Arg508Pro
NM_001304718.1:c.413G>C NP_001291647.1:p.Arg138Pro
XM_006717926.2:c.959G>C XP_006717989.1:p.Arg320Pro
XM_011539981.1:c.1004G>C XP_011538283.1:p.Arg335Pro
XM_011539982.1:c.908G>C XP_011538284.1:p.Arg303Pro
XR_945791.1:n.1574G>C
NM_000314.7:c.1004G>C NP_000305.3:p.Arg335Pro
NM_001304717.5:c.1523G>C NP_001291646.4:p.Arg508Pro
NM_001304718.2:c.413G>C NP_001291647.1:p.Arg138Pro
NM_000314.8:c.1004G>C MANE Select NP_000305.3:p.Arg335Pro