Canonical Allele Identifier: CA1926190100
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961070C= , CM000672.2:g.87961070C= GRCh38
NC_000010.10:g.89720827C= , CM000672.1:g.89720827C= GRCh37
NC_000010.9:g.89710807C= NCBI36
NG_007466.2:g.102632C= , LRG_311:g.102632C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1071C= ENSP00000514759.2:p.Asp357=
ENST00000710265.1:c.978C= ENSP00000518161.1:p.Asp326=
ENST00000472832.3:c.978C= ENSP00000483066.2:p.Asp326=
ENST00000688158.2:n.1713C=
ENST00000688922.2:c.*808C= ENSP00000508742.2:n.*808C=
ENST00000700021.1:c.933C= ENSP00000514757.1:p.Asp311=
ENST00000700022.1:c.*317C= ENSP00000514758.1:n.*317C=
ENST00000700023.1:n.2136C=
ENST00000700024.1:n.2370C=
ENST00000700025.1:n.1747C=
ENST00000700026.1:n.615C=
ENST00000706954.1:c.978C= ENSP00000516674.1:p.Asp326=
ENST00000706955.1:c.*1013C= ENSP00000516675.1:n.*1013C=
ENST00000686459.1:c.*564C= ENSP00000508909.1:n.*564C=
ENST00000688158.1:c.*1089C= ENSP00000509254.1:n.*1089C=
ENST00000688308.1:c.978C= ENSP00000508752.1:p.Asp326=
ENST00000688922.1:c.899C=
ENST00000693560.1:c.1497C= ENSP00000509861.1:p.Asp499=
ENST00000371953.8:c.978C= MANE Select ENSP00000361021.3:p.Asp326=
ENST00000371953.7:c.978C= ENSP00000361021.3:p.Asp326=
ENST00000472832.2:c.405C= ENSP00000483066.1:p.Asp135=
NM_000314.5:c.978C= NP_000305.3:p.Asp326=
NM_000314.6:c.978C= NP_000305.3:p.Asp326=
NM_001304717.2:c.1497C= NP_001291646.2:p.Asp499=
NM_001304718.1:c.387C= NP_001291647.1:p.Asp129=
XM_006717926.2:c.933C= XP_006717989.1:p.Asp311=
XM_011539981.1:c.978C= XP_011538283.1:p.Asp326=
XM_011539982.1:c.882C= XP_011538284.1:p.Asp294=
XR_945791.1:n.1548C=
NM_000314.7:c.978C= NP_000305.3:p.Asp326=
NM_001304717.5:c.1497C= NP_001291646.4:p.Asp499=
NM_001304718.2:c.387C= NP_001291647.1:p.Asp129=
NM_000314.8:c.978C= MANE Select NP_000305.3:p.Asp326=