Canonical Allele Identifier: CA2740097858
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 3066148
ClinVar RCV Id: RCV003991152

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957957_87957958insAAT , CM000672.2:g.87957957_87957958insAAT GRCh38
NC_000010.10:g.89717714_89717715insAAT , CM000672.1:g.89717714_89717715insAAT GRCh37
NC_000010.9:g.89707694_89707695insAAT NCBI36
NG_007466.2:g.99519_99520insAAT , LRG_311:g.99519_99520insAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.739_740insAAT ENSP00000514759.2:p.Leu247Ter
ENST00000710265.1:c.739_740insAAT ENSP00000518161.1:p.Leu247Ter
ENST00000472832.3:c.739_740insAAT ENSP00000483066.2:p.Leu247Ter
ENST00000688158.2:n.1474_1475insAAT
ENST00000688922.2:c.*569_*570insAAT ENSP00000508742.2:n.*569_*570insAAT
ENST00000700021.1:c.694_695insAAT ENSP00000514757.1:p.Leu232Ter
ENST00000700022.1:c.*78_*79insAAT ENSP00000514758.1:n.*78_*79insAAT
ENST00000700023.1:n.1897_1898insAAT
ENST00000700024.1:n.2131_2132insAAT
ENST00000700025.1:n.1508_1509insAAT
ENST00000700026.1:n.376_377insAAT
ENST00000700029.1:c.573_574insAAT
ENST00000706954.1:c.739_740insAAT ENSP00000516674.1:p.Leu247Ter
ENST00000706955.1:c.*774_*775insAAT ENSP00000516675.1:n.*774_*775insAAT
ENST00000686459.1:c.*325_*326insAAT ENSP00000508909.1:n.*325_*326insAAT
ENST00000688158.1:c.*850_*851insAAT ENSP00000509254.1:n.*850_*851insAAT
ENST00000688308.1:c.739_740insAAT ENSP00000508752.1:p.Leu247Ter
ENST00000688922.1:c.660_661insAAT
ENST00000693560.1:c.1258_1259insAAT ENSP00000509861.1:p.Leu420Ter
ENST00000371953.8:c.739_740insAAT MANE Select ENSP00000361021.3:p.Leu247Ter
ENST00000371953.7:c.739_740insAAT ENSP00000361021.3:p.Leu247Ter
ENST00000472832.2:c.166_167insAAT ENSP00000483066.1:p.Leu56Ter
NM_000314.5:c.739_740insAAT NP_000305.3:p.Leu247Ter
NM_000314.6:c.739_740insAAT NP_000305.3:p.Leu247Ter
NM_001304717.2:c.1258_1259insAAT NP_001291646.2:p.Leu420Ter
NM_001304718.1:c.148_149insAAT NP_001291647.1:p.Leu50Ter
XM_006717926.2:c.694_695insAAT XP_006717989.1:p.Leu232Ter
XM_011539981.1:c.739_740insAAT XP_011538283.1:p.Leu247Ter
XM_011539982.1:c.643_644insAAT XP_011538284.1:p.Leu215Ter
XR_945791.1:n.1309_1310insAAT
NM_000314.7:c.739_740insAAT NP_000305.3:p.Leu247Ter
NM_001304717.5:c.1258_1259insAAT NP_001291646.4:p.Leu420Ter
NM_001304718.2:c.148_149insAAT NP_001291647.1:p.Leu50Ter
NM_000314.8:c.739_740insAAT MANE Select NP_000305.3:p.Leu247Ter