Canonical Allele Identifier: CA1926182514
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952146A= , CM000672.2:g.87952146A= GRCh38
NC_000010.10:g.89711903A= , CM000672.1:g.89711903A= GRCh37
NC_000010.9:g.89701883A= NCBI36
NG_007466.2:g.93708A= , LRG_311:g.93708A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.521A= ENSP00000514759.2:p.Tyr174=
ENST00000710265.1:c.521A= ENSP00000518161.1:p.Tyr174=
ENST00000472832.3:c.521A= ENSP00000483066.2:p.Tyr174=
ENST00000688158.2:n.1256A=
ENST00000688922.2:c.*351A= ENSP00000508742.2:n.*351A=
ENST00000700021.1:c.476A= ENSP00000514757.1:p.Tyr159=
ENST00000700022.1:c.493-5707A= ENSP00000514758.1:n.493-5707A=
ENST00000700023.1:n.1679A=
ENST00000700024.1:n.1913A=
ENST00000700025.1:n.1290A=
ENST00000700029.1:c.355A=
ENST00000706954.1:c.521A= ENSP00000516674.1:p.Tyr174=
ENST00000706955.1:c.*556A= ENSP00000516675.1:n.*556A=
ENST00000686459.1:c.*107A= ENSP00000508909.1:n.*107A=
ENST00000688158.1:c.*632A= ENSP00000509254.1:n.*632A=
ENST00000688308.1:c.521A= ENSP00000508752.1:p.Tyr174=
ENST00000688922.1:c.442A=
ENST00000693560.1:c.1040A= ENSP00000509861.1:p.Tyr347=
ENST00000371953.8:c.521A= MANE Select ENSP00000361021.3:p.Tyr174=
ENST00000371953.7:c.521A= ENSP00000361021.3:p.Tyr174=
NM_000314.5:c.521A= NP_000305.3:p.Tyr174=
NM_000314.6:c.521A= NP_000305.3:p.Tyr174=
NM_001304717.2:c.1040A= NP_001291646.2:p.Tyr347=
NM_001304718.1:c.-71A= NP_001291647.1:n.-71A=
XM_006717926.2:c.476A= XP_006717989.1:p.Tyr159=
XM_011539981.1:c.521A= XP_011538283.1:p.Tyr174=
XM_011539982.1:c.425A= XP_011538284.1:p.Tyr142=
XR_945789.1:n.1392A=
XR_945790.1:n.1509A=
XR_945791.1:n.1205-5707A=
NM_000314.7:c.521A= NP_000305.3:p.Tyr174=
NM_001304717.5:c.1040A= NP_001291646.4:p.Tyr347=
NM_001304718.2:c.-71A= NP_001291647.1:n.-71A=
NM_000314.8:c.521A= MANE Select NP_000305.3:p.Tyr174=