Canonical Allele Identifier: CA1926182460
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952143G= , CM000672.2:g.87952143G= GRCh38
NC_000010.10:g.89711900G= , CM000672.1:g.89711900G= GRCh37
NC_000010.9:g.89701880G= NCBI36
NG_007466.2:g.93705G= , LRG_311:g.93705G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.518G= ENSP00000514759.2:p.Arg173=
ENST00000710265.1:c.518G= ENSP00000518161.1:p.Arg173=
ENST00000472832.3:c.518G= ENSP00000483066.2:p.Arg173=
ENST00000688158.2:n.1253G=
ENST00000688922.2:c.*348G= ENSP00000508742.2:n.*348G=
ENST00000700021.1:c.473G= ENSP00000514757.1:p.Arg158=
ENST00000700022.1:c.493-5710G= ENSP00000514758.1:n.493-5710G=
ENST00000700023.1:n.1676G=
ENST00000700024.1:n.1910G=
ENST00000700025.1:n.1287G=
ENST00000700029.1:c.352G=
ENST00000706954.1:c.518G= ENSP00000516674.1:p.Arg173=
ENST00000706955.1:c.*553G= ENSP00000516675.1:n.*553G=
ENST00000686459.1:c.*104G= ENSP00000508909.1:n.*104G=
ENST00000688158.1:c.*629G= ENSP00000509254.1:n.*629G=
ENST00000688308.1:c.518G= ENSP00000508752.1:p.Arg173=
ENST00000688922.1:c.439G=
ENST00000693560.1:c.1037G= ENSP00000509861.1:p.Arg346=
ENST00000371953.8:c.518G= MANE Select ENSP00000361021.3:p.Arg173=
ENST00000371953.7:c.518G= ENSP00000361021.3:p.Arg173=
NM_000314.5:c.518G= NP_000305.3:p.Arg173=
NM_000314.6:c.518G= NP_000305.3:p.Arg173=
NM_001304717.2:c.1037G= NP_001291646.2:p.Arg346=
NM_001304718.1:c.-74G= NP_001291647.1:n.-74G=
XM_006717926.2:c.473G= XP_006717989.1:p.Arg158=
XM_011539981.1:c.518G= XP_011538283.1:p.Arg173=
XM_011539982.1:c.422G= XP_011538284.1:p.Arg141=
XR_945789.1:n.1389G=
XR_945790.1:n.1506G=
XR_945791.1:n.1205-5710G=
NM_000314.7:c.518G= NP_000305.3:p.Arg173=
NM_001304717.5:c.1037G= NP_001291646.4:p.Arg346=
NM_001304718.2:c.-74G= NP_001291647.1:n.-74G=
NM_000314.8:c.518G= MANE Select NP_000305.3:p.Arg173=