Canonical Allele Identifier: CA891839836
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957957_87957958delinsAG , CM000672.2:g.87957957_87957958delinsAG GRCh38
NC_000010.10:g.89717714_89717715delinsAG , CM000672.1:g.89717714_89717715delinsAG GRCh37
NC_000010.9:g.89707694_89707695delinsAG NCBI36
NG_007466.2:g.99519_99520delinsAG , LRG_311:g.99519_99520delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.739_740delinsAG ENSP00000514759.2:p.Leu247Arg
ENST00000710265.1:c.739_740delinsAG ENSP00000518161.1:p.Leu247Arg
ENST00000472832.3:c.739_740delinsAG ENSP00000483066.2:p.Leu247Arg
ENST00000688158.2:n.1474_1475delinsAG
ENST00000688922.2:c.*569_*570delinsAG ENSP00000508742.2:n.*569_*570delinsAG
ENST00000700021.1:c.694_695delinsAG ENSP00000514757.1:p.Leu232Arg
ENST00000700022.1:c.*78_*79delinsAG ENSP00000514758.1:n.*78_*79delinsAG
ENST00000700023.1:n.1897_1898delinsAG
ENST00000700024.1:n.2131_2132delinsAG
ENST00000700025.1:n.1508_1509delinsAG
ENST00000700026.1:n.376_377delinsAG
ENST00000700029.1:c.573_574delinsAG
ENST00000706954.1:c.739_740delinsAG ENSP00000516674.1:p.Leu247Arg
ENST00000706955.1:c.*774_*775delinsAG ENSP00000516675.1:n.*774_*775delinsAG
ENST00000686459.1:c.*325_*326delinsAG ENSP00000508909.1:n.*325_*326delinsAG
ENST00000688158.1:c.*850_*851delinsAG ENSP00000509254.1:n.*850_*851delinsAG
ENST00000688308.1:c.739_740delinsAG ENSP00000508752.1:p.Leu247Arg
ENST00000688922.1:c.660_661delinsAG
ENST00000693560.1:c.1258_1259delinsAG ENSP00000509861.1:p.Leu420Arg
ENST00000371953.8:c.739_740delinsAG MANE Select ENSP00000361021.3:p.Leu247Arg
ENST00000371953.7:c.739_740delinsAG ENSP00000361021.3:p.Leu247Arg
ENST00000472832.2:c.166_167delinsAG ENSP00000483066.1:p.Leu56Arg
NM_000314.5:c.739_740delinsAG NP_000305.3:p.Leu247Arg
NM_000314.6:c.739_740delinsAG NP_000305.3:p.Leu247Arg
NM_001304717.2:c.1258_1259delinsAG NP_001291646.2:p.Leu420Arg
NM_001304718.1:c.148_149delinsAG NP_001291647.1:p.Leu50Arg
XM_006717926.2:c.694_695delinsAG XP_006717989.1:p.Leu232Arg
XM_011539981.1:c.739_740delinsAG XP_011538283.1:p.Leu247Arg
XM_011539982.1:c.643_644delinsAG XP_011538284.1:p.Leu215Arg
XR_945791.1:n.1309_1310delinsAG
NM_000314.7:c.739_740delinsAG NP_000305.3:p.Leu247Arg
NM_001304717.5:c.1258_1259delinsAG NP_001291646.4:p.Leu420Arg
NM_001304718.2:c.148_149delinsAG NP_001291647.1:p.Leu50Arg
NM_000314.8:c.739_740delinsAG MANE Select NP_000305.3:p.Leu247Arg