Canonical Allele Identifier: CA645369484
Gene: PTEN HGNC NCBI

Linked Data

ClinVar Variation Id: 428252
ClinVar RCV Id: RCV000490881
dbSNP Id: rs1114167666

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957956_87957961del , CM000672.2:g.87957956_87957961del GRCh38
NC_000010.10:g.89717713_89717718del , CM000672.1:g.89717713_89717718del GRCh37
NC_000010.9:g.89707693_89707698del NCBI36
NG_007466.2:g.99518_99523del , LRG_311:g.99518_99523del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.738_743del ENSP00000514759.2:p.Leu247_Pro248del
ENST00000710265.1:c.738_743del ENSP00000518161.1:p.Leu247_Pro248del
ENST00000472832.3:c.738_743del ENSP00000483066.2:p.Leu247_Pro248del
ENST00000688158.2:n.1473_1478del
ENST00000688922.2:c.*568_*573del ENSP00000508742.2:n.*568_*573del
ENST00000700021.1:c.693_698del ENSP00000514757.1:p.Leu232_Pro233del
ENST00000700022.1:c.*77_*82del ENSP00000514758.1:n.*77_*82del
ENST00000700023.1:n.1896_1901del
ENST00000700024.1:n.2130_2135del
ENST00000700025.1:n.1507_1512del
ENST00000700026.1:n.375_380del
ENST00000700029.1:c.572_577del
ENST00000706954.1:c.738_743del ENSP00000516674.1:p.Leu247_Pro248del
ENST00000706955.1:c.*773_*778del ENSP00000516675.1:n.*773_*778del
ENST00000686459.1:c.*324_*329del ENSP00000508909.1:n.*324_*329del
ENST00000688158.1:c.*849_*854del ENSP00000509254.1:n.*849_*854del
ENST00000688308.1:c.738_743del ENSP00000508752.1:p.Leu247_Pro248del
ENST00000688922.1:c.659_664del
ENST00000693560.1:c.1257_1262del ENSP00000509861.1:p.Leu420_Pro421del
ENST00000371953.8:c.738_743del MANE Select ENSP00000361021.3:p.Leu247_Pro248del
ENST00000371953.7:c.738_743del ENSP00000361021.3:p.Leu247_Pro248del
ENST00000472832.2:c.165_170del ENSP00000483066.1:p.Leu56_Pro57del
NM_000314.5:c.738_743del NP_000305.3:p.Leu247_Pro248del
NM_000314.6:c.738_743del NP_000305.3:p.Leu247_Pro248del
NM_001304717.2:c.1257_1262del NP_001291646.2:p.Leu420_Pro421del
NM_001304718.1:c.147_152del NP_001291647.1:p.Leu50_Pro51del
XM_006717926.2:c.693_698del XP_006717989.1:p.Leu232_Pro233del
XM_011539981.1:c.738_743del XP_011538283.1:p.Leu247_Pro248del
XM_011539982.1:c.642_647del XP_011538284.1:p.Leu215_Pro216del
XR_945791.1:n.1308_1313del
NM_000314.7:c.738_743del NP_000305.3:p.Leu247_Pro248del
NM_001304717.5:c.1257_1262del NP_001291646.4:p.Leu420_Pro421del
NM_001304718.2:c.147_152del NP_001291647.1:p.Leu50_Pro51del
NM_000314.8:c.738_743del MANE Select NP_000305.3:p.Leu247_Pro248del