Canonical Allele Identifier: CA1926162990
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87925552C= , CM000672.2:g.87925552C= GRCh38
NC_000010.10:g.89685309C= , CM000672.1:g.89685309C= GRCh37
NC_000010.9:g.89675289C= NCBI36
NG_007466.2:g.67114C= , LRG_311:g.67114C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.204C= ENSP00000514759.2:p.Tyr68=
ENST00000710265.1:c.204C= ENSP00000518161.1:p.Tyr68=
ENST00000472832.3:c.204C= ENSP00000483066.2:p.Tyr68=
ENST00000688158.2:n.939C=
ENST00000688922.2:c.204C= ENSP00000508742.2:p.Tyr68=
ENST00000700021.1:c.165-5494C= ENSP00000514757.1:n.165-5494C=
ENST00000700022.1:c.204C= ENSP00000514758.1:p.Tyr68=
ENST00000700029.1:c.38C=
ENST00000706954.1:c.204C= ENSP00000516674.1:p.Tyr68=
ENST00000706955.1:c.*239C= ENSP00000516675.1:n.*239C=
ENST00000686459.1:c.204C= ENSP00000508909.1:p.Tyr68=
ENST00000688158.1:c.*315C= ENSP00000509254.1:n.*315C=
ENST00000688308.1:c.204C= ENSP00000508752.1:p.Tyr68=
ENST00000688922.1:c.73C=
ENST00000693560.1:c.723C= ENSP00000509861.1:p.Tyr241=
ENST00000371953.8:c.204C= MANE Select ENSP00000361021.3:p.Tyr68=
ENST00000371953.7:c.204C= ENSP00000361021.3:p.Tyr68=
ENST00000498703.1:n.30C=
ENST00000610634.1:c.102C= ENSP00000477517.1:p.Tyr34=
NM_000314.5:c.204C= NP_000305.3:p.Tyr68=
NM_000314.6:c.204C= NP_000305.3:p.Tyr68=
NM_001304717.2:c.723C= NP_001291646.2:p.Tyr241=
NM_001304718.1:c.-541-5494C= NP_001291647.1:n.-541-5494C=
XM_006717926.2:c.165-5494C= XP_006717989.1:n.165-5494C=
XM_011539981.1:c.204C= XP_011538283.1:p.Tyr68=
XM_011539982.1:c.108C= XP_011538284.1:p.Tyr36=
XR_945789.1:n.916C=
XR_945790.1:n.916C=
XR_945791.1:n.916C=
NM_000314.7:c.204C= NP_000305.3:p.Tyr68=
NM_001304717.5:c.723C= NP_001291646.4:p.Tyr241=
NM_001304718.2:c.-541-5494C= NP_001291647.1:n.-541-5494C=
NM_000314.8:c.204C= MANE Select NP_000305.3:p.Tyr68=