Canonical Allele Identifier: CA645554061
Gene: PTEN HGNC NCBI

Linked Data

COSMIC: COSM921129

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87957982_87957984del , CM000672.2:g.87957982_87957984del GRCh38
NC_000010.10:g.89717739_89717741del , CM000672.1:g.89717739_89717741del GRCh37
NC_000010.9:g.89707719_89707721del NCBI36
NG_007466.2:g.99544_99546del , LRG_311:g.99544_99546del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.764_766del ENSP00000514759.2:p.Val255del
ENST00000710265.1:c.764_766del ENSP00000518161.1:p.Val255del
ENST00000472832.3:c.764_766del ENSP00000483066.2:p.Val255del
ENST00000688158.2:n.1499_1501del
ENST00000688922.2:c.*594_*596del ENSP00000508742.2:n.*594_*596del
ENST00000700021.1:c.719_721del ENSP00000514757.1:p.Val240del
ENST00000700022.1:c.*103_*105del ENSP00000514758.1:n.*103_*105del
ENST00000700023.1:n.1922_1924del
ENST00000700024.1:n.2156_2158del
ENST00000700025.1:n.1533_1535del
ENST00000700026.1:n.401_403del
ENST00000700029.1:c.598_600del
ENST00000706954.1:c.764_766del ENSP00000516674.1:p.Val255del
ENST00000706955.1:c.*799_*801del ENSP00000516675.1:n.*799_*801del
ENST00000686459.1:c.*350_*352del ENSP00000508909.1:n.*350_*352del
ENST00000688158.1:c.*875_*877del ENSP00000509254.1:n.*875_*877del
ENST00000688308.1:c.764_766del ENSP00000508752.1:p.Val255del
ENST00000688922.1:c.685_687del
ENST00000693560.1:c.1283_1285del ENSP00000509861.1:p.Val428del
ENST00000371953.8:c.764_766del MANE Select ENSP00000361021.3:p.Val255del
ENST00000371953.7:c.764_766del ENSP00000361021.3:p.Val255del
ENST00000472832.2:c.191_193del ENSP00000483066.1:p.Val64del
NM_000314.5:c.764_766del NP_000305.3:p.Val255del
NM_000314.6:c.764_766del NP_000305.3:p.Val255del
NM_001304717.2:c.1283_1285del NP_001291646.2:p.Val428del
NM_001304718.1:c.173_175del NP_001291647.1:p.Val58del
XM_006717926.2:c.719_721del XP_006717989.1:p.Val240del
XM_011539981.1:c.764_766del XP_011538283.1:p.Val255del
XM_011539982.1:c.668_670del XP_011538284.1:p.Val223del
XR_945791.1:n.1334_1336del
NM_000314.7:c.764_766del NP_000305.3:p.Val255del
NM_001304717.5:c.1283_1285del NP_001291646.4:p.Val428del
NM_001304718.2:c.173_175del NP_001291647.1:p.Val58del
NM_000314.8:c.764_766del MANE Select NP_000305.3:p.Val255del