Canonical Allele Identifier: CA377484756
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957855C>A , CM000672.2:g.87957855C>A GRCh38
NC_000010.10:g.89717612C>A , CM000672.1:g.89717612C>A GRCh37
NC_000010.9:g.89707592C>A NCBI36
NG_007466.2:g.99417C>A , LRG_311:g.99417C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.637C>A ENSP00000514759.2:p.Pro213Thr
ENST00000710265.1:c.637C>A ENSP00000518161.1:p.Pro213Thr
ENST00000472832.3:c.637C>A ENSP00000483066.2:p.Pro213Thr
ENST00000688158.2:n.1372C>A
ENST00000688922.2:c.*467C>A ENSP00000508742.2:n.*467C>A
ENST00000700021.1:c.592C>A ENSP00000514757.1:p.Pro198Thr
ENST00000700022.1:c.495C>A ENSP00000514758.1:p.Ile165=
ENST00000700023.1:n.1795C>A
ENST00000700024.1:n.2029C>A
ENST00000700025.1:n.1406C>A
ENST00000700026.1:n.274C>A
ENST00000700029.1:c.471C>A
ENST00000706954.1:c.637C>A ENSP00000516674.1:p.Pro213Thr
ENST00000706955.1:c.*672C>A ENSP00000516675.1:n.*672C>A
ENST00000686459.1:c.*223C>A ENSP00000508909.1:n.*223C>A
ENST00000688158.1:c.*748C>A ENSP00000509254.1:n.*748C>A
ENST00000688308.1:c.637C>A ENSP00000508752.1:p.Pro213Thr
ENST00000688922.1:c.558C>A
ENST00000693560.1:c.1156C>A ENSP00000509861.1:p.Pro386Thr
ENST00000371953.8:c.637C>A MANE Select ENSP00000361021.3:p.Pro213Thr
ENST00000371953.7:c.637C>A ENSP00000361021.3:p.Pro213Thr
ENST00000472832.2:c.64C>A ENSP00000483066.1:p.Pro22Thr
NM_000314.5:c.637C>A NP_000305.3:p.Pro213Thr
NM_000314.6:c.637C>A NP_000305.3:p.Pro213Thr
NM_001304717.2:c.1156C>A NP_001291646.2:p.Pro386Thr
NM_001304718.1:c.46C>A NP_001291647.1:p.Pro16Thr
XM_006717926.2:c.592C>A XP_006717989.1:p.Pro198Thr
XM_011539981.1:c.637C>A XP_011538283.1:p.Pro213Thr
XM_011539982.1:c.541C>A XP_011538284.1:p.Pro181Thr
XR_945791.1:n.1207C>A
NM_000314.7:c.637C>A NP_000305.3:p.Pro213Thr
NM_001304717.5:c.1156C>A NP_001291646.4:p.Pro386Thr
NM_001304718.2:c.46C>A NP_001291647.1:p.Pro16Thr
NM_000314.8:c.637C>A MANE Select NP_000305.3:p.Pro213Thr