Canonical Allele Identifier: CA645554014
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957952_87957953insTTAGTTCCCTCAG , CM000672.2:g.87957952_87957953insTTAGTTCCCTCAG GRCh38
NC_000010.10:g.89717709_89717710insTTAGTTCCCTCAG , CM000672.1:g.89717709_89717710insTTAGTTCCCTCAG GRCh37
NC_000010.9:g.89707689_89707690insTTAGTTCCCTCAG NCBI36
NG_007466.2:g.99514_99515insTTAGTTCCCTCAG , LRG_311:g.99514_99515insTTAGTTCCCTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.734_735insTTAGTTCCCTCAG ENSP00000514759.2:p.Gln245HisfsTer2
ENST00000710265.1:c.734_735insTTAGTTCCCTCAG ENSP00000518161.1:p.Gln245HisfsTer2
ENST00000472832.3:c.734_735insTTAGTTCCCTCAG ENSP00000483066.2:p.Gln245HisfsTer2
ENST00000688158.2:n.1469_1470insTTAGTTCCCTCAG
ENST00000688922.2:c.*564_*565insTTAGTTCCCTCAG ENSP00000508742.2:n.*564_*565insTTAGTTCCCTCAG
ENST00000700021.1:c.689_690insTTAGTTCCCTCAG ENSP00000514757.1:p.Gln230HisfsTer2
ENST00000700022.1:c.*73_*74insTTAGTTCCCTCAG ENSP00000514758.1:n.*73_*74insTTAGTTCCCTCAG
ENST00000700023.1:n.1892_1893insTTAGTTCCCTCAG
ENST00000700024.1:n.2126_2127insTTAGTTCCCTCAG
ENST00000700025.1:n.1503_1504insTTAGTTCCCTCAG
ENST00000700026.1:n.371_372insTTAGTTCCCTCAG
ENST00000700029.1:c.568_569insTTAGTTCCCTCAG
ENST00000706954.1:c.734_735insTTAGTTCCCTCAG ENSP00000516674.1:p.Gln245HisfsTer2
ENST00000706955.1:c.*769_*770insTTAGTTCCCTCAG ENSP00000516675.1:n.*769_*770insTTAGTTCCCTCAG
ENST00000686459.1:c.*320_*321insTTAGTTCCCTCAG ENSP00000508909.1:n.*320_*321insTTAGTTCCCTCAG
ENST00000688158.1:c.*845_*846insTTAGTTCCCTCAG ENSP00000509254.1:n.*845_*846insTTAGTTCCCTCAG
ENST00000688308.1:c.734_735insTTAGTTCCCTCAG ENSP00000508752.1:p.Gln245HisfsTer2
ENST00000688922.1:c.655_656insTTAGTTCCCTCAG
ENST00000693560.1:c.1253_1254insTTAGTTCCCTCAG ENSP00000509861.1:p.Gln418HisfsTer2
ENST00000371953.8:c.734_735insTTAGTTCCCTCAG MANE Select ENSP00000361021.3:p.Gln245HisfsTer2
ENST00000371953.7:c.734_735insTTAGTTCCCTCAG ENSP00000361021.3:p.Gln245HisfsTer2
ENST00000472832.2:c.161_162insTTAGTTCCCTCAG ENSP00000483066.1:p.Gln54HisfsTer2
NM_000314.5:c.734_735insTTAGTTCCCTCAG NP_000305.3:p.Gln245HisfsTer2
NM_000314.6:c.734_735insTTAGTTCCCTCAG NP_000305.3:p.Gln245HisfsTer2
NM_001304717.2:c.1253_1254insTTAGTTCCCTCAG NP_001291646.2:p.Gln418HisfsTer2
NM_001304718.1:c.143_144insTTAGTTCCCTCAG NP_001291647.1:p.Gln48HisfsTer2
XM_006717926.2:c.689_690insTTAGTTCCCTCAG XP_006717989.1:p.Gln230HisfsTer2
XM_011539981.1:c.734_735insTTAGTTCCCTCAG XP_011538283.1:p.Gln245HisfsTer2
XM_011539982.1:c.638_639insTTAGTTCCCTCAG XP_011538284.1:p.Gln213HisfsTer2
XR_945791.1:n.1304_1305insTTAGTTCCCTCAG
NM_000314.7:c.734_735insTTAGTTCCCTCAG NP_000305.3:p.Gln245HisfsTer2
NM_001304717.5:c.1253_1254insTTAGTTCCCTCAG NP_001291646.4:p.Gln418HisfsTer2
NM_001304718.2:c.143_144insTTAGTTCCCTCAG NP_001291647.1:p.Gln48HisfsTer2
NM_000314.8:c.734_735insTTAGTTCCCTCAG MANE Select NP_000305.3:p.Gln245HisfsTer2