Canonical Allele Identifier: CA891840804
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957951_87957952delinsGC , CM000672.2:g.87957951_87957952delinsGC GRCh38
NC_000010.10:g.89717708_89717709delinsGC , CM000672.1:g.89717708_89717709delinsGC GRCh37
NC_000010.9:g.89707688_89707689delinsGC NCBI36
NG_007466.2:g.99513_99514delinsGC , LRG_311:g.99513_99514delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.733_734delinsGC ENSP00000514759.2:p.Gln245Ala
ENST00000710265.1:c.733_734delinsGC ENSP00000518161.1:p.Gln245Ala
ENST00000472832.3:c.733_734delinsGC ENSP00000483066.2:p.Gln245Ala
ENST00000688158.2:n.1468_1469delinsGC
ENST00000688922.2:c.*563_*564delinsGC ENSP00000508742.2:n.*563_*564delinsGC
ENST00000700021.1:c.688_689delinsGC ENSP00000514757.1:p.Gln230Ala
ENST00000700022.1:c.*72_*73delinsGC ENSP00000514758.1:n.*72_*73delinsGC
ENST00000700023.1:n.1891_1892delinsGC
ENST00000700024.1:n.2125_2126delinsGC
ENST00000700025.1:n.1502_1503delinsGC
ENST00000700026.1:n.370_371delinsGC
ENST00000700029.1:c.567_568delinsGC
ENST00000706954.1:c.733_734delinsGC ENSP00000516674.1:p.Gln245Ala
ENST00000706955.1:c.*768_*769delinsGC ENSP00000516675.1:n.*768_*769delinsGC
ENST00000686459.1:c.*319_*320delinsGC ENSP00000508909.1:n.*319_*320delinsGC
ENST00000688158.1:c.*844_*845delinsGC ENSP00000509254.1:n.*844_*845delinsGC
ENST00000688308.1:c.733_734delinsGC ENSP00000508752.1:p.Gln245Ala
ENST00000688922.1:c.654_655delinsGC
ENST00000693560.1:c.1252_1253delinsGC ENSP00000509861.1:p.Gln418Ala
ENST00000371953.8:c.733_734delinsGC MANE Select ENSP00000361021.3:p.Gln245Ala
ENST00000371953.7:c.733_734delinsGC ENSP00000361021.3:p.Gln245Ala
ENST00000472832.2:c.160_161delinsGC ENSP00000483066.1:p.Gln54Ala
NM_000314.5:c.733_734delinsGC NP_000305.3:p.Gln245Ala
NM_000314.6:c.733_734delinsGC NP_000305.3:p.Gln245Ala
NM_001304717.2:c.1252_1253delinsGC NP_001291646.2:p.Gln418Ala
NM_001304718.1:c.142_143delinsGC NP_001291647.1:p.Gln48Ala
XM_006717926.2:c.688_689delinsGC XP_006717989.1:p.Gln230Ala
XM_011539981.1:c.733_734delinsGC XP_011538283.1:p.Gln245Ala
XM_011539982.1:c.637_638delinsGC XP_011538284.1:p.Gln213Ala
XR_945791.1:n.1303_1304delinsGC
NM_000314.7:c.733_734delinsGC NP_000305.3:p.Gln245Ala
NM_001304717.5:c.1252_1253delinsGC NP_001291646.4:p.Gln418Ala
NM_001304718.2:c.142_143delinsGC NP_001291647.1:p.Gln48Ala
NM_000314.8:c.733_734delinsGC MANE Select NP_000305.3:p.Gln245Ala