Canonical Allele Identifier: CA060691
Gene: PTEN HGNC NCBI

Linked Data

dbSNP Id: rs755112271

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87960861_87960865del , CM000672.2:g.87960861_87960865del GRCh38
NC_000010.10:g.89720618_89720622del , CM000672.1:g.89720618_89720622del GRCh37
NC_000010.9:g.89710598_89710602del NCBI36
NG_007466.2:g.102423_102427del , LRG_311:g.102423_102427del

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.895-33_895-29del ENSP00000514759.2:n.895-33_895-29del
ENST00000710265.1:c.802-33_802-29del ENSP00000518161.1:n.802-33_802-29del
ENST00000472832.3:c.802-33_802-29del ENSP00000483066.2:n.802-33_802-29del
ENST00000688158.2:n.1537-33_1537-29del
ENST00000688922.2:c.*632-33_*632-29del ENSP00000508742.2:n.*632-33_*632-29del
ENST00000700021.1:c.757-33_757-29del ENSP00000514757.1:n.757-33_757-29del
ENST00000700022.1:c.*141-33_*141-29del ENSP00000514758.1:n.*141-33_*141-29del
ENST00000700023.1:n.1960-33_1960-29del
ENST00000700024.1:n.2194-33_2194-29del
ENST00000700025.1:n.1571-33_1571-29del
ENST00000700026.1:n.439-33_439-29del
ENST00000700029.1:c.729-33_729-29del
ENST00000706954.1:c.802-33_802-29del ENSP00000516674.1:n.802-33_802-29del
ENST00000706955.1:c.*837-33_*837-29del ENSP00000516675.1:n.*837-33_*837-29del
ENST00000686459.1:c.*388-33_*388-29del ENSP00000508909.1:n.*388-33_*388-29del
ENST00000688158.1:c.*913-33_*913-29del ENSP00000509254.1:n.*913-33_*913-29del
ENST00000688308.1:c.802-33_802-29del ENSP00000508752.1:n.802-33_802-29del
ENST00000688922.1:c.723-33_723-29del
ENST00000693560.1:c.1321-33_1321-29del ENSP00000509861.1:n.1321-33_1321-29del
ENST00000371953.8:c.802-33_802-29del MANE Select ENSP00000361021.3:n.802-33_802-29del
ENST00000371953.7:c.802-33_802-29del ENSP00000361021.3:n.802-33_802-29del
ENST00000472832.2:c.229-33_229-29del ENSP00000483066.1:n.229-33_229-29del
NM_000314.5:c.802-33_802-29del NP_000305.3:n.802-33_802-29del
NM_000314.6:c.802-33_802-29del NP_000305.3:n.802-33_802-29del
NM_001304717.2:c.1321-33_1321-29del NP_001291646.2:n.1321-33_1321-29del
NM_001304718.1:c.211-33_211-29del NP_001291647.1:n.211-33_211-29del
XM_006717926.2:c.757-33_757-29del XP_006717989.1:n.757-33_757-29del
XM_011539981.1:c.802-33_802-29del XP_011538283.1:n.802-33_802-29del
XM_011539982.1:c.706-33_706-29del XP_011538284.1:n.706-33_706-29del
XR_945791.1:n.1372-33_1372-29del
NM_000314.7:c.802-33_802-29del NP_000305.3:n.802-33_802-29del
NM_001304717.5:c.1321-33_1321-29del NP_001291646.4:n.1321-33_1321-29del
NM_001304718.2:c.211-33_211-29del NP_001291647.1:n.211-33_211-29del
NM_000314.8:c.802-33_802-29del MANE Select NP_000305.3:n.802-33_802-29del