Canonical Allele Identifier: CA891840822
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957957_87957958delinsGG , CM000672.2:g.87957957_87957958delinsGG GRCh38
NC_000010.10:g.89717714_89717715delinsGG , CM000672.1:g.89717714_89717715delinsGG GRCh37
NC_000010.9:g.89707694_89707695delinsGG NCBI36
NG_007466.2:g.99519_99520delinsGG , LRG_311:g.99519_99520delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.739_740delinsGG ENSP00000514759.2:p.Leu247Gly
ENST00000710265.1:c.739_740delinsGG ENSP00000518161.1:p.Leu247Gly
ENST00000472832.3:c.739_740delinsGG ENSP00000483066.2:p.Leu247Gly
ENST00000688158.2:n.1474_1475delinsGG
ENST00000688922.2:c.*569_*570delinsGG ENSP00000508742.2:n.*569_*570delinsGG
ENST00000700021.1:c.694_695delinsGG ENSP00000514757.1:p.Leu232Gly
ENST00000700022.1:c.*78_*79delinsGG ENSP00000514758.1:n.*78_*79delinsGG
ENST00000700023.1:n.1897_1898delinsGG
ENST00000700024.1:n.2131_2132delinsGG
ENST00000700025.1:n.1508_1509delinsGG
ENST00000700026.1:n.376_377delinsGG
ENST00000700029.1:c.573_574delinsGG
ENST00000706954.1:c.739_740delinsGG ENSP00000516674.1:p.Leu247Gly
ENST00000706955.1:c.*774_*775delinsGG ENSP00000516675.1:n.*774_*775delinsGG
ENST00000686459.1:c.*325_*326delinsGG ENSP00000508909.1:n.*325_*326delinsGG
ENST00000688158.1:c.*850_*851delinsGG ENSP00000509254.1:n.*850_*851delinsGG
ENST00000688308.1:c.739_740delinsGG ENSP00000508752.1:p.Leu247Gly
ENST00000688922.1:c.660_661delinsGG
ENST00000693560.1:c.1258_1259delinsGG ENSP00000509861.1:p.Leu420Gly
ENST00000371953.8:c.739_740delinsGG MANE Select ENSP00000361021.3:p.Leu247Gly
ENST00000371953.7:c.739_740delinsGG ENSP00000361021.3:p.Leu247Gly
ENST00000472832.2:c.166_167delinsGG ENSP00000483066.1:p.Leu56Gly
NM_000314.5:c.739_740delinsGG NP_000305.3:p.Leu247Gly
NM_000314.6:c.739_740delinsGG NP_000305.3:p.Leu247Gly
NM_001304717.2:c.1258_1259delinsGG NP_001291646.2:p.Leu420Gly
NM_001304718.1:c.148_149delinsGG NP_001291647.1:p.Leu50Gly
XM_006717926.2:c.694_695delinsGG XP_006717989.1:p.Leu232Gly
XM_011539981.1:c.739_740delinsGG XP_011538283.1:p.Leu247Gly
XM_011539982.1:c.643_644delinsGG XP_011538284.1:p.Leu215Gly
XR_945791.1:n.1309_1310delinsGG
NM_000314.7:c.739_740delinsGG NP_000305.3:p.Leu247Gly
NM_001304717.5:c.1258_1259delinsGG NP_001291646.4:p.Leu420Gly
NM_001304718.2:c.148_149delinsGG NP_001291647.1:p.Leu50Gly
NM_000314.8:c.739_740delinsGG MANE Select NP_000305.3:p.Leu247Gly