Canonical Allele Identifier: CA645554015
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957952_87957953insTAACTTGTTTG , CM000672.2:g.87957952_87957953insTAACTTGTTTG GRCh38
NC_000010.10:g.89717709_89717710insTAACTTGTTTG , CM000672.1:g.89717709_89717710insTAACTTGTTTG GRCh37
NC_000010.9:g.89707689_89707690insTAACTTGTTTG NCBI36
NG_007466.2:g.99514_99515insTAACTTGTTTG , LRG_311:g.99514_99515insTAACTTGTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.734_735insTAACTTGTTTG ENSP00000514759.2:p.Gln245HisfsTer15
ENST00000710265.1:c.734_735insTAACTTGTTTG ENSP00000518161.1:p.Gln245HisfsTer15
ENST00000472832.3:c.734_735insTAACTTGTTTG ENSP00000483066.2:p.Gln245HisfsTer15
ENST00000688158.2:n.1469_1470insTAACTTGTTTG
ENST00000688922.2:c.*564_*565insTAACTTGTTTG ENSP00000508742.2:n.*564_*565insTAACTTGTTTG
ENST00000700021.1:c.689_690insTAACTTGTTTG ENSP00000514757.1:p.Gln230HisfsTer15
ENST00000700022.1:c.*73_*74insTAACTTGTTTG ENSP00000514758.1:n.*73_*74insTAACTTGTTTG
ENST00000700023.1:n.1892_1893insTAACTTGTTTG
ENST00000700024.1:n.2126_2127insTAACTTGTTTG
ENST00000700025.1:n.1503_1504insTAACTTGTTTG
ENST00000700026.1:n.371_372insTAACTTGTTTG
ENST00000700029.1:c.568_569insTAACTTGTTTG
ENST00000706954.1:c.734_735insTAACTTGTTTG ENSP00000516674.1:p.Gln245HisfsTer15
ENST00000706955.1:c.*769_*770insTAACTTGTTTG ENSP00000516675.1:n.*769_*770insTAACTTGTTTG
ENST00000686459.1:c.*320_*321insTAACTTGTTTG ENSP00000508909.1:n.*320_*321insTAACTTGTTTG
ENST00000688158.1:c.*845_*846insTAACTTGTTTG ENSP00000509254.1:n.*845_*846insTAACTTGTTTG
ENST00000688308.1:c.734_735insTAACTTGTTTG ENSP00000508752.1:p.Gln245HisfsTer15
ENST00000688922.1:c.655_656insTAACTTGTTTG
ENST00000693560.1:c.1253_1254insTAACTTGTTTG ENSP00000509861.1:p.Gln418HisfsTer15
ENST00000371953.8:c.734_735insTAACTTGTTTG MANE Select ENSP00000361021.3:p.Gln245HisfsTer15
ENST00000371953.7:c.734_735insTAACTTGTTTG ENSP00000361021.3:p.Gln245HisfsTer15
ENST00000472832.2:c.161_162insTAACTTGTTTG ENSP00000483066.1:p.Gln54HisfsTer15
NM_000314.5:c.734_735insTAACTTGTTTG NP_000305.3:p.Gln245HisfsTer15
NM_000314.6:c.734_735insTAACTTGTTTG NP_000305.3:p.Gln245HisfsTer15
NM_001304717.2:c.1253_1254insTAACTTGTTTG NP_001291646.2:p.Gln418HisfsTer15
NM_001304718.1:c.143_144insTAACTTGTTTG NP_001291647.1:p.Gln48HisfsTer15
XM_006717926.2:c.689_690insTAACTTGTTTG XP_006717989.1:p.Gln230HisfsTer15
XM_011539981.1:c.734_735insTAACTTGTTTG XP_011538283.1:p.Gln245HisfsTer15
XM_011539982.1:c.638_639insTAACTTGTTTG XP_011538284.1:p.Gln213HisfsTer15
XR_945791.1:n.1304_1305insTAACTTGTTTG
NM_000314.7:c.734_735insTAACTTGTTTG NP_000305.3:p.Gln245HisfsTer15
NM_001304717.5:c.1253_1254insTAACTTGTTTG NP_001291646.4:p.Gln418HisfsTer15
NM_001304718.2:c.143_144insTAACTTGTTTG NP_001291647.1:p.Gln48HisfsTer15
NM_000314.8:c.734_735insTAACTTGTTTG MANE Select NP_000305.3:p.Gln245HisfsTer15