Canonical Allele Identifier: CA1926188628
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87958018A= , CM000672.2:g.87958018A= GRCh38
NC_000010.10:g.89717775A= , CM000672.1:g.89717775A= GRCh37
NC_000010.9:g.89707755A= NCBI36
NG_007466.2:g.99580A= , LRG_311:g.99580A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.800A= ENSP00000514759.2:p.Lys267=
ENST00000710265.1:c.800A= ENSP00000518161.1:p.Lys267=
ENST00000472832.3:c.800A= ENSP00000483066.2:p.Lys267=
ENST00000688158.2:n.1535A=
ENST00000688922.2:c.*630A= ENSP00000508742.2:n.*630A=
ENST00000700021.1:c.755A= ENSP00000514757.1:p.Lys252=
ENST00000700022.1:c.*139A= ENSP00000514758.1:n.*139A=
ENST00000700023.1:n.1958A=
ENST00000700024.1:n.2192A=
ENST00000700025.1:n.1569A=
ENST00000700026.1:n.437A=
ENST00000700029.1:c.634A=
ENST00000706954.1:c.800A= ENSP00000516674.1:p.Lys267=
ENST00000706955.1:c.*835A= ENSP00000516675.1:n.*835A=
ENST00000686459.1:c.*386A= ENSP00000508909.1:n.*386A=
ENST00000688158.1:c.*911A= ENSP00000509254.1:n.*911A=
ENST00000688308.1:c.800A= ENSP00000508752.1:p.Lys267=
ENST00000688922.1:c.721A=
ENST00000693560.1:c.1319A= ENSP00000509861.1:p.Lys440=
ENST00000371953.8:c.800A= MANE Select ENSP00000361021.3:p.Lys267=
ENST00000371953.7:c.800A= ENSP00000361021.3:p.Lys267=
ENST00000472832.2:c.227A= ENSP00000483066.1:p.Lys76=
NM_000314.5:c.800A= NP_000305.3:p.Lys267=
NM_000314.6:c.800A= NP_000305.3:p.Lys267=
NM_001304717.2:c.1319A= NP_001291646.2:p.Lys440=
NM_001304718.1:c.209A= NP_001291647.1:p.Lys70=
XM_006717926.2:c.755A= XP_006717989.1:p.Lys252=
XM_011539981.1:c.800A= XP_011538283.1:p.Lys267=
XM_011539982.1:c.704A= XP_011538284.1:p.Lys235=
XR_945791.1:n.1370A=
NM_000314.7:c.800A= NP_000305.3:p.Lys267=
NM_001304717.5:c.1319A= NP_001291646.4:p.Lys440=
NM_001304718.2:c.209A= NP_001291647.1:p.Lys70=
NM_000314.8:c.800A= MANE Select NP_000305.3:p.Lys267=