Canonical Allele Identifier: CA1926188569
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957952A= , CM000672.2:g.87957952A= GRCh38
NC_000010.10:g.89717709A= , CM000672.1:g.89717709A= GRCh37
NC_000010.9:g.89707689A= NCBI36
NG_007466.2:g.99514A= , LRG_311:g.99514A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.734A= ENSP00000514759.2:p.Gln245=
ENST00000710265.1:c.734A= ENSP00000518161.1:p.Gln245=
ENST00000472832.3:c.734A= ENSP00000483066.2:p.Gln245=
ENST00000688158.2:n.1469A=
ENST00000688922.2:c.*564A= ENSP00000508742.2:n.*564A=
ENST00000700021.1:c.689A= ENSP00000514757.1:p.Gln230=
ENST00000700022.1:c.*73A= ENSP00000514758.1:n.*73A=
ENST00000700023.1:n.1892A=
ENST00000700024.1:n.2126A=
ENST00000700025.1:n.1503A=
ENST00000700026.1:n.371A=
ENST00000700029.1:c.568A=
ENST00000706954.1:c.734A= ENSP00000516674.1:p.Gln245=
ENST00000706955.1:c.*769A= ENSP00000516675.1:n.*769A=
ENST00000686459.1:c.*320A= ENSP00000508909.1:n.*320A=
ENST00000688158.1:c.*845A= ENSP00000509254.1:n.*845A=
ENST00000688308.1:c.734A= ENSP00000508752.1:p.Gln245=
ENST00000688922.1:c.655A=
ENST00000693560.1:c.1253A= ENSP00000509861.1:p.Gln418=
ENST00000371953.8:c.734A= MANE Select ENSP00000361021.3:p.Gln245=
ENST00000371953.7:c.734A= ENSP00000361021.3:p.Gln245=
ENST00000472832.2:c.161A= ENSP00000483066.1:p.Gln54=
NM_000314.5:c.734A= NP_000305.3:p.Gln245=
NM_000314.6:c.734A= NP_000305.3:p.Gln245=
NM_001304717.2:c.1253A= NP_001291646.2:p.Gln418=
NM_001304718.1:c.143A= NP_001291647.1:p.Gln48=
XM_006717926.2:c.689A= XP_006717989.1:p.Gln230=
XM_011539981.1:c.734A= XP_011538283.1:p.Gln245=
XM_011539982.1:c.638A= XP_011538284.1:p.Gln213=
XR_945791.1:n.1304A=
NM_000314.7:c.734A= NP_000305.3:p.Gln245=
NM_001304717.5:c.1253A= NP_001291646.4:p.Gln418=
NM_001304718.2:c.143A= NP_001291647.1:p.Gln48=
NM_000314.8:c.734A= MANE Select NP_000305.3:p.Gln245=