Canonical Allele Identifier: CA645554037
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM30560

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957956_87957957insCACTCAC , CM000672.2:g.87957956_87957957insCACTCAC GRCh38
NC_000010.10:g.89717713_89717714insCACTCAC , CM000672.1:g.89717713_89717714insCACTCAC GRCh37
NC_000010.9:g.89707693_89707694insCACTCAC NCBI36
NG_007466.2:g.99518_99519insCACTCAC , LRG_311:g.99518_99519insCACTCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.738_739insCACTCAC ENSP00000514759.2:p.Leu247HisfsTer8
ENST00000710265.1:c.738_739insCACTCAC ENSP00000518161.1:p.Leu247HisfsTer8
ENST00000472832.3:c.738_739insCACTCAC ENSP00000483066.2:p.Leu247HisfsTer8
ENST00000688158.2:n.1473_1474insCACTCAC
ENST00000688922.2:c.*568_*569insCACTCAC ENSP00000508742.2:n.*568_*569insCACTCAC
ENST00000700021.1:c.693_694insCACTCAC ENSP00000514757.1:p.Leu232HisfsTer8
ENST00000700022.1:c.*77_*78insCACTCAC ENSP00000514758.1:n.*77_*78insCACTCAC
ENST00000700023.1:n.1896_1897insCACTCAC
ENST00000700024.1:n.2130_2131insCACTCAC
ENST00000700025.1:n.1507_1508insCACTCAC
ENST00000700026.1:n.375_376insCACTCAC
ENST00000700029.1:c.572_573insCACTCAC
ENST00000706954.1:c.738_739insCACTCAC ENSP00000516674.1:p.Leu247HisfsTer8
ENST00000706955.1:c.*773_*774insCACTCAC ENSP00000516675.1:n.*773_*774insCACTCAC
ENST00000686459.1:c.*324_*325insCACTCAC ENSP00000508909.1:n.*324_*325insCACTCAC
ENST00000688158.1:c.*849_*850insCACTCAC ENSP00000509254.1:n.*849_*850insCACTCAC
ENST00000688308.1:c.738_739insCACTCAC ENSP00000508752.1:p.Leu247HisfsTer8
ENST00000688922.1:c.659_660insCACTCAC
ENST00000693560.1:c.1257_1258insCACTCAC ENSP00000509861.1:p.Leu420HisfsTer8
ENST00000371953.8:c.738_739insCACTCAC MANE Select ENSP00000361021.3:p.Leu247HisfsTer8
ENST00000371953.7:c.738_739insCACTCAC ENSP00000361021.3:p.Leu247HisfsTer8
ENST00000472832.2:c.165_166insCACTCAC ENSP00000483066.1:p.Leu56HisfsTer8
NM_000314.5:c.738_739insCACTCAC NP_000305.3:p.Leu247HisfsTer8
NM_000314.6:c.738_739insCACTCAC NP_000305.3:p.Leu247HisfsTer8
NM_001304717.2:c.1257_1258insCACTCAC NP_001291646.2:p.Leu420HisfsTer8
NM_001304718.1:c.147_148insCACTCAC NP_001291647.1:p.Leu50HisfsTer8
XM_006717926.2:c.693_694insCACTCAC XP_006717989.1:p.Leu232HisfsTer8
XM_011539981.1:c.738_739insCACTCAC XP_011538283.1:p.Leu247HisfsTer8
XM_011539982.1:c.642_643insCACTCAC XP_011538284.1:p.Leu215HisfsTer8
XR_945791.1:n.1308_1309insCACTCAC
NM_000314.7:c.738_739insCACTCAC NP_000305.3:p.Leu247HisfsTer8
NM_001304717.5:c.1257_1258insCACTCAC NP_001291646.4:p.Leu420HisfsTer8
NM_001304718.2:c.147_148insCACTCAC NP_001291647.1:p.Leu50HisfsTer8
NM_000314.8:c.738_739insCACTCAC MANE Select NP_000305.3:p.Leu247HisfsTer8