Canonical Allele Identifier: CA1926188518
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957885A= , CM000672.2:g.87957885A= GRCh38
NC_000010.10:g.89717642A= , CM000672.1:g.89717642A= GRCh37
NC_000010.9:g.89707622A= NCBI36
NG_007466.2:g.99447A= , LRG_311:g.99447A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.667A= ENSP00000514759.2:p.Lys223=
ENST00000710265.1:c.667A= ENSP00000518161.1:p.Lys223=
ENST00000472832.3:c.667A= ENSP00000483066.2:p.Lys223=
ENST00000688158.2:n.1402A=
ENST00000688922.2:c.*497A= ENSP00000508742.2:n.*497A=
ENST00000700021.1:c.622A= ENSP00000514757.1:p.Lys208=
ENST00000700022.1:c.*6A= ENSP00000514758.1:n.*6A=
ENST00000700023.1:n.1825A=
ENST00000700024.1:n.2059A=
ENST00000700025.1:n.1436A=
ENST00000700026.1:n.304A=
ENST00000700029.1:c.501A=
ENST00000706954.1:c.667A= ENSP00000516674.1:p.Lys223=
ENST00000706955.1:c.*702A= ENSP00000516675.1:n.*702A=
ENST00000686459.1:c.*253A= ENSP00000508909.1:n.*253A=
ENST00000688158.1:c.*778A= ENSP00000509254.1:n.*778A=
ENST00000688308.1:c.667A= ENSP00000508752.1:p.Lys223=
ENST00000688922.1:c.588A=
ENST00000693560.1:c.1186A= ENSP00000509861.1:p.Lys396=
ENST00000371953.8:c.667A= MANE Select ENSP00000361021.3:p.Lys223=
ENST00000371953.7:c.667A= ENSP00000361021.3:p.Lys223=
ENST00000472832.2:c.94A= ENSP00000483066.1:p.Lys32=
NM_000314.5:c.667A= NP_000305.3:p.Lys223=
NM_000314.6:c.667A= NP_000305.3:p.Lys223=
NM_001304717.2:c.1186A= NP_001291646.2:p.Lys396=
NM_001304718.1:c.76A= NP_001291647.1:p.Lys26=
XM_006717926.2:c.622A= XP_006717989.1:p.Lys208=
XM_011539981.1:c.667A= XP_011538283.1:p.Lys223=
XM_011539982.1:c.571A= XP_011538284.1:p.Lys191=
XR_945791.1:n.1237A=
NM_000314.7:c.667A= NP_000305.3:p.Lys223=
NM_001304717.5:c.1186A= NP_001291646.4:p.Lys396=
NM_001304718.2:c.76A= NP_001291647.1:p.Lys26=
NM_000314.8:c.667A= MANE Select NP_000305.3:p.Lys223=