Canonical Allele Identifier: CA645554017
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM36018

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957956_87957957insGGCCCG , CM000672.2:g.87957956_87957957insGGCCCG GRCh38
NC_000010.10:g.89717713_89717714insGGCCCG , CM000672.1:g.89717713_89717714insGGCCCG GRCh37
NC_000010.9:g.89707693_89707694insGGCCCG NCBI36
NG_007466.2:g.99518_99519insGGCCCG , LRG_311:g.99518_99519insGGCCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.738_739insGGCCCG ENSP00000514759.2:p.Pro246_Leu247insGlyPro
ENST00000710265.1:c.738_739insGGCCCG ENSP00000518161.1:p.Pro246_Leu247insGlyPro
ENST00000472832.3:c.738_739insGGCCCG ENSP00000483066.2:p.Pro246_Leu247insGlyPro
ENST00000688158.2:n.1473_1474insGGCCCG
ENST00000688922.2:c.*568_*569insGGCCCG ENSP00000508742.2:n.*568_*569insGGCCCG
ENST00000700021.1:c.693_694insGGCCCG ENSP00000514757.1:p.Pro231_Leu232insGlyPro
ENST00000700022.1:c.*77_*78insGGCCCG ENSP00000514758.1:n.*77_*78insGGCCCG
ENST00000700023.1:n.1896_1897insGGCCCG
ENST00000700024.1:n.2130_2131insGGCCCG
ENST00000700025.1:n.1507_1508insGGCCCG
ENST00000700026.1:n.375_376insGGCCCG
ENST00000700029.1:c.572_573insGGCCCG
ENST00000706954.1:c.738_739insGGCCCG ENSP00000516674.1:p.Pro246_Leu247insGlyPro
ENST00000706955.1:c.*773_*774insGGCCCG ENSP00000516675.1:n.*773_*774insGGCCCG
ENST00000686459.1:c.*324_*325insGGCCCG ENSP00000508909.1:n.*324_*325insGGCCCG
ENST00000688158.1:c.*849_*850insGGCCCG ENSP00000509254.1:n.*849_*850insGGCCCG
ENST00000688308.1:c.738_739insGGCCCG ENSP00000508752.1:p.Pro246_Leu247insGlyPro
ENST00000688922.1:c.659_660insGGCCCG
ENST00000693560.1:c.1257_1258insGGCCCG ENSP00000509861.1:p.Pro419_Leu420insGlyPro
ENST00000371953.8:c.738_739insGGCCCG MANE Select ENSP00000361021.3:p.Pro246_Leu247insGlyPro
ENST00000371953.7:c.738_739insGGCCCG ENSP00000361021.3:p.Pro246_Leu247insGlyPro
ENST00000472832.2:c.165_166insGGCCCG ENSP00000483066.1:p.Pro55_Leu56insGlyPro
NM_000314.5:c.738_739insGGCCCG NP_000305.3:p.Pro246_Leu247insGlyPro
NM_000314.6:c.738_739insGGCCCG NP_000305.3:p.Pro246_Leu247insGlyPro
NM_001304717.2:c.1257_1258insGGCCCG NP_001291646.2:p.Pro419_Leu420insGlyPro
NM_001304718.1:c.147_148insGGCCCG NP_001291647.1:p.Pro49_Leu50insGlyPro
XM_006717926.2:c.693_694insGGCCCG XP_006717989.1:p.Pro231_Leu232insGlyPro
XM_011539981.1:c.738_739insGGCCCG XP_011538283.1:p.Pro246_Leu247insGlyPro
XM_011539982.1:c.642_643insGGCCCG XP_011538284.1:p.Pro214_Leu215insGlyPro
XR_945791.1:n.1308_1309insGGCCCG
NM_000314.7:c.738_739insGGCCCG NP_000305.3:p.Pro246_Leu247insGlyPro
NM_001304717.5:c.1257_1258insGGCCCG NP_001291646.4:p.Pro419_Leu420insGlyPro
NM_001304718.2:c.147_148insGGCCCG NP_001291647.1:p.Pro49_Leu50insGlyPro
NM_000314.8:c.738_739insGGCCCG MANE Select NP_000305.3:p.Pro246_Leu247insGlyPro