Canonical Allele Identifier: CA891839886
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957966_87957968delinsCAA , CM000672.2:g.87957966_87957968delinsCAA GRCh38
NC_000010.10:g.89717723_89717725delinsCAA , CM000672.1:g.89717723_89717725delinsCAA GRCh37
NC_000010.9:g.89707703_89707705delinsCAA NCBI36
NG_007466.2:g.99528_99530delinsCAA , LRG_311:g.99528_99530delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.748_750delinsCAA ENSP00000514759.2:p.Cys250Gln
ENST00000710265.1:c.748_750delinsCAA ENSP00000518161.1:p.Cys250Gln
ENST00000472832.3:c.748_750delinsCAA ENSP00000483066.2:p.Cys250Gln
ENST00000688158.2:n.1483_1485delinsCAA
ENST00000688922.2:c.*578_*580delinsCAA ENSP00000508742.2:n.*578_*580delinsCAA
ENST00000700021.1:c.703_705delinsCAA ENSP00000514757.1:p.Cys235Gln
ENST00000700022.1:c.*87_*89delinsCAA ENSP00000514758.1:n.*87_*89delinsCAA
ENST00000700023.1:n.1906_1908delinsCAA
ENST00000700024.1:n.2140_2142delinsCAA
ENST00000700025.1:n.1517_1519delinsCAA
ENST00000700026.1:n.385_387delinsCAA
ENST00000700029.1:c.582_584delinsCAA
ENST00000706954.1:c.748_750delinsCAA ENSP00000516674.1:p.Cys250Gln
ENST00000706955.1:c.*783_*785delinsCAA ENSP00000516675.1:n.*783_*785delinsCAA
ENST00000686459.1:c.*334_*336delinsCAA ENSP00000508909.1:n.*334_*336delinsCAA
ENST00000688158.1:c.*859_*861delinsCAA ENSP00000509254.1:n.*859_*861delinsCAA
ENST00000688308.1:c.748_750delinsCAA ENSP00000508752.1:p.Cys250Gln
ENST00000688922.1:c.669_671delinsCAA
ENST00000693560.1:c.1267_1269delinsCAA ENSP00000509861.1:p.Cys423Gln
ENST00000371953.8:c.748_750delinsCAA MANE Select ENSP00000361021.3:p.Cys250Gln
ENST00000371953.7:c.748_750delinsCAA ENSP00000361021.3:p.Cys250Gln
ENST00000472832.2:c.175_177delinsCAA ENSP00000483066.1:p.Cys59Gln
NM_000314.5:c.748_750delinsCAA NP_000305.3:p.Cys250Gln
NM_000314.6:c.748_750delinsCAA NP_000305.3:p.Cys250Gln
NM_001304717.2:c.1267_1269delinsCAA NP_001291646.2:p.Cys423Gln
NM_001304718.1:c.157_159delinsCAA NP_001291647.1:p.Cys53Gln
XM_006717926.2:c.703_705delinsCAA XP_006717989.1:p.Cys235Gln
XM_011539981.1:c.748_750delinsCAA XP_011538283.1:p.Cys250Gln
XM_011539982.1:c.652_654delinsCAA XP_011538284.1:p.Cys218Gln
XR_945791.1:n.1318_1320delinsCAA
NM_000314.7:c.748_750delinsCAA NP_000305.3:p.Cys250Gln
NM_001304717.5:c.1267_1269delinsCAA NP_001291646.4:p.Cys423Gln
NM_001304718.2:c.157_159delinsCAA NP_001291647.1:p.Cys53Gln
NM_000314.8:c.748_750delinsCAA MANE Select NP_000305.3:p.Cys250Gln