Canonical Allele Identifier: CA2610047248
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957956_87957957insGGCCG , CM000672.2:g.87957956_87957957insGGCCG GRCh38
NC_000010.10:g.89717713_89717714insGGCCG , CM000672.1:g.89717713_89717714insGGCCG GRCh37
NC_000010.9:g.89707693_89707694insGGCCG NCBI36
NG_007466.2:g.99518_99519insGGCCG , LRG_311:g.99518_99519insGGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.738_739insGGCCG ENSP00000514759.2:p.Leu247GlyfsTer11
ENST00000710265.1:c.738_739insGGCCG ENSP00000518161.1:p.Leu247GlyfsTer11
ENST00000472832.3:c.738_739insGGCCG ENSP00000483066.2:p.Leu247GlyfsTer11
ENST00000688158.2:n.1473_1474insGGCCG
ENST00000688922.2:c.*568_*569insGGCCG ENSP00000508742.2:n.*568_*569insGGCCG
ENST00000700021.1:c.693_694insGGCCG ENSP00000514757.1:p.Leu232GlyfsTer11
ENST00000700022.1:c.*77_*78insGGCCG ENSP00000514758.1:n.*77_*78insGGCCG
ENST00000700023.1:n.1896_1897insGGCCG
ENST00000700024.1:n.2130_2131insGGCCG
ENST00000700025.1:n.1507_1508insGGCCG
ENST00000700026.1:n.375_376insGGCCG
ENST00000700029.1:c.572_573insGGCCG
ENST00000706954.1:c.738_739insGGCCG ENSP00000516674.1:p.Leu247GlyfsTer11
ENST00000706955.1:c.*773_*774insGGCCG ENSP00000516675.1:n.*773_*774insGGCCG
ENST00000686459.1:c.*324_*325insGGCCG ENSP00000508909.1:n.*324_*325insGGCCG
ENST00000688158.1:c.*849_*850insGGCCG ENSP00000509254.1:n.*849_*850insGGCCG
ENST00000688308.1:c.738_739insGGCCG ENSP00000508752.1:p.Leu247GlyfsTer11
ENST00000688922.1:c.659_660insGGCCG
ENST00000693560.1:c.1257_1258insGGCCG ENSP00000509861.1:p.Leu420GlyfsTer11
ENST00000371953.8:c.738_739insGGCCG MANE Select ENSP00000361021.3:p.Leu247GlyfsTer11
ENST00000371953.7:c.738_739insGGCCG ENSP00000361021.3:p.Leu247GlyfsTer11
ENST00000472832.2:c.165_166insGGCCG ENSP00000483066.1:p.Leu56GlyfsTer11
NM_000314.5:c.738_739insGGCCG NP_000305.3:p.Leu247GlyfsTer11
NM_000314.6:c.738_739insGGCCG NP_000305.3:p.Leu247GlyfsTer11
NM_001304717.2:c.1257_1258insGGCCG NP_001291646.2:p.Leu420GlyfsTer11
NM_001304718.1:c.147_148insGGCCG NP_001291647.1:p.Leu50GlyfsTer11
XM_006717926.2:c.693_694insGGCCG XP_006717989.1:p.Leu232GlyfsTer11
XM_011539981.1:c.738_739insGGCCG XP_011538283.1:p.Leu247GlyfsTer11
XM_011539982.1:c.642_643insGGCCG XP_011538284.1:p.Leu215GlyfsTer11
XR_945791.1:n.1308_1309insGGCCG
NM_000314.7:c.738_739insGGCCG NP_000305.3:p.Leu247GlyfsTer11
NM_001304717.5:c.1257_1258insGGCCG NP_001291646.4:p.Leu420GlyfsTer11
NM_001304718.2:c.147_148insGGCCG NP_001291647.1:p.Leu50GlyfsTer11
NM_000314.8:c.738_739insGGCCG MANE Select NP_000305.3:p.Leu247GlyfsTer11