Canonical Allele Identifier: CA377484324
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs2132269174

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952151T>A , CM000672.2:g.87952151T>A GRCh38
NC_000010.10:g.89711908T>A , CM000672.1:g.89711908T>A GRCh37
NC_000010.9:g.89701888T>A NCBI36
NG_007466.2:g.93713T>A , LRG_311:g.93713T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.526T>A ENSP00000514759.2:p.Tyr176Asn
ENST00000710265.1:c.526T>A ENSP00000518161.1:p.Tyr176Asn
ENST00000472832.3:c.526T>A ENSP00000483066.2:p.Tyr176Asn
ENST00000688158.2:n.1261T>A
ENST00000688922.2:c.*356T>A ENSP00000508742.2:n.*356T>A
ENST00000700021.1:c.481T>A ENSP00000514757.1:p.Tyr161Asn
ENST00000700022.1:c.493-5702T>A ENSP00000514758.1:n.493-5702T>A
ENST00000700023.1:n.1684T>A
ENST00000700024.1:n.1918T>A
ENST00000700025.1:n.1295T>A
ENST00000700029.1:c.360T>A
ENST00000706954.1:c.526T>A ENSP00000516674.1:p.Tyr176Asn
ENST00000706955.1:c.*561T>A ENSP00000516675.1:n.*561T>A
ENST00000686459.1:c.*112T>A ENSP00000508909.1:n.*112T>A
ENST00000688158.1:c.*637T>A ENSP00000509254.1:n.*637T>A
ENST00000688308.1:c.526T>A ENSP00000508752.1:p.Tyr176Asn
ENST00000688922.1:c.447T>A
ENST00000693560.1:c.1045T>A ENSP00000509861.1:p.Tyr349Asn
ENST00000371953.8:c.526T>A MANE Select ENSP00000361021.3:p.Tyr176Asn
ENST00000371953.7:c.526T>A ENSP00000361021.3:p.Tyr176Asn
NM_000314.5:c.526T>A NP_000305.3:p.Tyr176Asn
NM_000314.6:c.526T>A NP_000305.3:p.Tyr176Asn
NM_001304717.2:c.1045T>A NP_001291646.2:p.Tyr349Asn
NM_001304718.1:c.-66T>A NP_001291647.1:n.-66T>A
XM_006717926.2:c.481T>A XP_006717989.1:p.Tyr161Asn
XM_011539981.1:c.526T>A XP_011538283.1:p.Tyr176Asn
XM_011539982.1:c.430T>A XP_011538284.1:p.Tyr144Asn
XR_945789.1:n.1397T>A
XR_945790.1:n.1514T>A
XR_945791.1:n.1205-5702T>A
NM_000314.7:c.526T>A NP_000305.3:p.Tyr176Asn
NM_001304717.5:c.1045T>A NP_001291646.4:p.Tyr349Asn
NM_001304718.2:c.-66T>A NP_001291647.1:n.-66T>A
NM_000314.8:c.526T>A MANE Select NP_000305.3:p.Tyr176Asn