Canonical Allele Identifier: CA1926182480
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87952144C= , CM000672.2:g.87952144C= GRCh38
NC_000010.10:g.89711901C= , CM000672.1:g.89711901C= GRCh37
NC_000010.9:g.89701881C= NCBI36
NG_007466.2:g.93706C= , LRG_311:g.93706C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.519C= ENSP00000514759.2:p.Arg173=
ENST00000710265.1:c.519C= ENSP00000518161.1:p.Arg173=
ENST00000472832.3:c.519C= ENSP00000483066.2:p.Arg173=
ENST00000688158.2:n.1254C=
ENST00000688922.2:c.*349C= ENSP00000508742.2:n.*349C=
ENST00000700021.1:c.474C= ENSP00000514757.1:p.Arg158=
ENST00000700022.1:c.493-5709C= ENSP00000514758.1:n.493-5709C=
ENST00000700023.1:n.1677C=
ENST00000700024.1:n.1911C=
ENST00000700025.1:n.1288C=
ENST00000700029.1:c.353C=
ENST00000706954.1:c.519C= ENSP00000516674.1:p.Arg173=
ENST00000706955.1:c.*554C= ENSP00000516675.1:n.*554C=
ENST00000686459.1:c.*105C= ENSP00000508909.1:n.*105C=
ENST00000688158.1:c.*630C= ENSP00000509254.1:n.*630C=
ENST00000688308.1:c.519C= ENSP00000508752.1:p.Arg173=
ENST00000688922.1:c.440C=
ENST00000693560.1:c.1038C= ENSP00000509861.1:p.Arg346=
ENST00000371953.8:c.519C= MANE Select ENSP00000361021.3:p.Arg173=
ENST00000371953.7:c.519C= ENSP00000361021.3:p.Arg173=
NM_000314.5:c.519C= NP_000305.3:p.Arg173=
NM_000314.6:c.519C= NP_000305.3:p.Arg173=
NM_001304717.2:c.1038C= NP_001291646.2:p.Arg346=
NM_001304718.1:c.-73C= NP_001291647.1:n.-73C=
XM_006717926.2:c.474C= XP_006717989.1:p.Arg158=
XM_011539981.1:c.519C= XP_011538283.1:p.Arg173=
XM_011539982.1:c.423C= XP_011538284.1:p.Arg141=
XR_945789.1:n.1390C=
XR_945790.1:n.1507C=
XR_945791.1:n.1205-5709C=
NM_000314.7:c.519C= NP_000305.3:p.Arg173=
NM_001304717.5:c.1038C= NP_001291646.4:p.Arg346=
NM_001304718.2:c.-73C= NP_001291647.1:n.-73C=
NM_000314.8:c.519C= MANE Select NP_000305.3:p.Arg173=