Canonical Allele Identifier: CA645554016
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957952_87957953insTGAGTTCCCTCAG , CM000672.2:g.87957952_87957953insTGAGTTCCCTCAG GRCh38
NC_000010.10:g.89717709_89717710insTGAGTTCCCTCAG , CM000672.1:g.89717709_89717710insTGAGTTCCCTCAG GRCh37
NC_000010.9:g.89707689_89707690insTGAGTTCCCTCAG NCBI36
NG_007466.2:g.99514_99515insTGAGTTCCCTCAG , LRG_311:g.99514_99515insTGAGTTCCCTCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.734_735insTGAGTTCCCTCAG ENSP00000514759.2:p.Gln245HisfsTer12
ENST00000710265.1:c.734_735insTGAGTTCCCTCAG ENSP00000518161.1:p.Gln245HisfsTer12
ENST00000472832.3:c.734_735insTGAGTTCCCTCAG ENSP00000483066.2:p.Gln245HisfsTer12
ENST00000688158.2:n.1469_1470insTGAGTTCCCTCAG
ENST00000688922.2:c.*564_*565insTGAGTTCCCTCAG ENSP00000508742.2:n.*564_*565insTGAGTTCCCTCAG
ENST00000700021.1:c.689_690insTGAGTTCCCTCAG ENSP00000514757.1:p.Gln230HisfsTer12
ENST00000700022.1:c.*73_*74insTGAGTTCCCTCAG ENSP00000514758.1:n.*73_*74insTGAGTTCCCTCAG
ENST00000700023.1:n.1892_1893insTGAGTTCCCTCAG
ENST00000700024.1:n.2126_2127insTGAGTTCCCTCAG
ENST00000700025.1:n.1503_1504insTGAGTTCCCTCAG
ENST00000700026.1:n.371_372insTGAGTTCCCTCAG
ENST00000700029.1:c.568_569insTGAGTTCCCTCAG
ENST00000706954.1:c.734_735insTGAGTTCCCTCAG ENSP00000516674.1:p.Gln245HisfsTer12
ENST00000706955.1:c.*769_*770insTGAGTTCCCTCAG ENSP00000516675.1:n.*769_*770insTGAGTTCCCTCAG
ENST00000686459.1:c.*320_*321insTGAGTTCCCTCAG ENSP00000508909.1:n.*320_*321insTGAGTTCCCTCAG
ENST00000688158.1:c.*845_*846insTGAGTTCCCTCAG ENSP00000509254.1:n.*845_*846insTGAGTTCCCTCAG
ENST00000688308.1:c.734_735insTGAGTTCCCTCAG ENSP00000508752.1:p.Gln245HisfsTer12
ENST00000688922.1:c.655_656insTGAGTTCCCTCAG
ENST00000693560.1:c.1253_1254insTGAGTTCCCTCAG ENSP00000509861.1:p.Gln418HisfsTer12
ENST00000371953.8:c.734_735insTGAGTTCCCTCAG MANE Select ENSP00000361021.3:p.Gln245HisfsTer12
ENST00000371953.7:c.734_735insTGAGTTCCCTCAG ENSP00000361021.3:p.Gln245HisfsTer12
ENST00000472832.2:c.161_162insTGAGTTCCCTCAG ENSP00000483066.1:p.Gln54HisfsTer12
NM_000314.5:c.734_735insTGAGTTCCCTCAG NP_000305.3:p.Gln245HisfsTer12
NM_000314.6:c.734_735insTGAGTTCCCTCAG NP_000305.3:p.Gln245HisfsTer12
NM_001304717.2:c.1253_1254insTGAGTTCCCTCAG NP_001291646.2:p.Gln418HisfsTer12
NM_001304718.1:c.143_144insTGAGTTCCCTCAG NP_001291647.1:p.Gln48HisfsTer12
XM_006717926.2:c.689_690insTGAGTTCCCTCAG XP_006717989.1:p.Gln230HisfsTer12
XM_011539981.1:c.734_735insTGAGTTCCCTCAG XP_011538283.1:p.Gln245HisfsTer12
XM_011539982.1:c.638_639insTGAGTTCCCTCAG XP_011538284.1:p.Gln213HisfsTer12
XR_945791.1:n.1304_1305insTGAGTTCCCTCAG
NM_000314.7:c.734_735insTGAGTTCCCTCAG NP_000305.3:p.Gln245HisfsTer12
NM_001304717.5:c.1253_1254insTGAGTTCCCTCAG NP_001291646.4:p.Gln418HisfsTer12
NM_001304718.2:c.143_144insTGAGTTCCCTCAG NP_001291647.1:p.Gln48HisfsTer12
NM_000314.8:c.734_735insTGAGTTCCCTCAG MANE Select NP_000305.3:p.Gln245HisfsTer12