Canonical Allele Identifier: CA891839890
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957966_87957967delinsAT , CM000672.2:g.87957966_87957967delinsAT GRCh38
NC_000010.10:g.89717723_89717724delinsAT , CM000672.1:g.89717723_89717724delinsAT GRCh37
NC_000010.9:g.89707703_89707704delinsAT NCBI36
NG_007466.2:g.99528_99529delinsAT , LRG_311:g.99528_99529delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.748_749delinsAT ENSP00000514759.2:p.Cys250Ile
ENST00000710265.1:c.748_749delinsAT ENSP00000518161.1:p.Cys250Ile
ENST00000472832.3:c.748_749delinsAT ENSP00000483066.2:p.Cys250Ile
ENST00000688158.2:n.1483_1484delinsAT
ENST00000688922.2:c.*578_*579delinsAT ENSP00000508742.2:n.*578_*579delinsAT
ENST00000700021.1:c.703_704delinsAT ENSP00000514757.1:p.Cys235Ile
ENST00000700022.1:c.*87_*88delinsAT ENSP00000514758.1:n.*87_*88delinsAT
ENST00000700023.1:n.1906_1907delinsAT
ENST00000700024.1:n.2140_2141delinsAT
ENST00000700025.1:n.1517_1518delinsAT
ENST00000700026.1:n.385_386delinsAT
ENST00000700029.1:c.582_583delinsAT
ENST00000706954.1:c.748_749delinsAT ENSP00000516674.1:p.Cys250Ile
ENST00000706955.1:c.*783_*784delinsAT ENSP00000516675.1:n.*783_*784delinsAT
ENST00000686459.1:c.*334_*335delinsAT ENSP00000508909.1:n.*334_*335delinsAT
ENST00000688158.1:c.*859_*860delinsAT ENSP00000509254.1:n.*859_*860delinsAT
ENST00000688308.1:c.748_749delinsAT ENSP00000508752.1:p.Cys250Ile
ENST00000688922.1:c.669_670delinsAT
ENST00000693560.1:c.1267_1268delinsAT ENSP00000509861.1:p.Cys423Ile
ENST00000371953.8:c.748_749delinsAT MANE Select ENSP00000361021.3:p.Cys250Ile
ENST00000371953.7:c.748_749delinsAT ENSP00000361021.3:p.Cys250Ile
ENST00000472832.2:c.175_176delinsAT ENSP00000483066.1:p.Cys59Ile
NM_000314.5:c.748_749delinsAT NP_000305.3:p.Cys250Ile
NM_000314.6:c.748_749delinsAT NP_000305.3:p.Cys250Ile
NM_001304717.2:c.1267_1268delinsAT NP_001291646.2:p.Cys423Ile
NM_001304718.1:c.157_158delinsAT NP_001291647.1:p.Cys53Ile
XM_006717926.2:c.703_704delinsAT XP_006717989.1:p.Cys235Ile
XM_011539981.1:c.748_749delinsAT XP_011538283.1:p.Cys250Ile
XM_011539982.1:c.652_653delinsAT XP_011538284.1:p.Cys218Ile
XR_945791.1:n.1318_1319delinsAT
NM_000314.7:c.748_749delinsAT NP_000305.3:p.Cys250Ile
NM_001304717.5:c.1267_1268delinsAT NP_001291646.4:p.Cys423Ile
NM_001304718.2:c.157_158delinsAT NP_001291647.1:p.Cys53Ile
NM_000314.8:c.748_749delinsAT MANE Select NP_000305.3:p.Cys250Ile