Canonical Allele Identifier: CA645554027
Gene: PTEN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957956_87957957insATAACGTG , CM000672.2:g.87957956_87957957insATAACGTG GRCh38
NC_000010.10:g.89717713_89717714insATAACGTG , CM000672.1:g.89717713_89717714insATAACGTG GRCh37
NC_000010.9:g.89707693_89707694insATAACGTG NCBI36
NG_007466.2:g.99518_99519insATAACGTG , LRG_311:g.99518_99519insATAACGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.738_739insATAACGTG ENSP00000514759.2:p.Leu247IlefsTer12
ENST00000710265.1:c.738_739insATAACGTG ENSP00000518161.1:p.Leu247IlefsTer12
ENST00000472832.3:c.738_739insATAACGTG ENSP00000483066.2:p.Leu247IlefsTer12
ENST00000688158.2:n.1473_1474insATAACGTG
ENST00000688922.2:c.*568_*569insATAACGTG ENSP00000508742.2:n.*568_*569insATAACGTG
ENST00000700021.1:c.693_694insATAACGTG ENSP00000514757.1:p.Leu232IlefsTer12
ENST00000700022.1:c.*77_*78insATAACGTG ENSP00000514758.1:n.*77_*78insATAACGTG
ENST00000700023.1:n.1896_1897insATAACGTG
ENST00000700024.1:n.2130_2131insATAACGTG
ENST00000700025.1:n.1507_1508insATAACGTG
ENST00000700026.1:n.375_376insATAACGTG
ENST00000700029.1:c.572_573insATAACGTG
ENST00000706954.1:c.738_739insATAACGTG ENSP00000516674.1:p.Leu247IlefsTer12
ENST00000706955.1:c.*773_*774insATAACGTG ENSP00000516675.1:n.*773_*774insATAACGTG
ENST00000686459.1:c.*324_*325insATAACGTG ENSP00000508909.1:n.*324_*325insATAACGTG
ENST00000688158.1:c.*849_*850insATAACGTG ENSP00000509254.1:n.*849_*850insATAACGTG
ENST00000688308.1:c.738_739insATAACGTG ENSP00000508752.1:p.Leu247IlefsTer12
ENST00000688922.1:c.659_660insATAACGTG
ENST00000693560.1:c.1257_1258insATAACGTG ENSP00000509861.1:p.Leu420IlefsTer12
ENST00000371953.8:c.738_739insATAACGTG MANE Select ENSP00000361021.3:p.Leu247IlefsTer12
ENST00000371953.7:c.738_739insATAACGTG ENSP00000361021.3:p.Leu247IlefsTer12
ENST00000472832.2:c.165_166insATAACGTG ENSP00000483066.1:p.Leu56IlefsTer12
NM_000314.5:c.738_739insATAACGTG NP_000305.3:p.Leu247IlefsTer12
NM_000314.6:c.738_739insATAACGTG NP_000305.3:p.Leu247IlefsTer12
NM_001304717.2:c.1257_1258insATAACGTG NP_001291646.2:p.Leu420IlefsTer12
NM_001304718.1:c.147_148insATAACGTG NP_001291647.1:p.Leu50IlefsTer12
XM_006717926.2:c.693_694insATAACGTG XP_006717989.1:p.Leu232IlefsTer12
XM_011539981.1:c.738_739insATAACGTG XP_011538283.1:p.Leu247IlefsTer12
XM_011539982.1:c.642_643insATAACGTG XP_011538284.1:p.Leu215IlefsTer12
XR_945791.1:n.1308_1309insATAACGTG
NM_000314.7:c.738_739insATAACGTG NP_000305.3:p.Leu247IlefsTer12
NM_001304717.5:c.1257_1258insATAACGTG NP_001291646.4:p.Leu420IlefsTer12
NM_001304718.2:c.147_148insATAACGTG NP_001291647.1:p.Leu50IlefsTer12
NM_000314.8:c.738_739insATAACGTG MANE Select NP_000305.3:p.Leu247IlefsTer12