Canonical Allele Identifier: CA1926190110
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961089_87961107delinsGCCAACCGATACTTTTCTC , CM000672.2:g.87961089_87961107delinsGCCAACCGATACTTTTCTC GRCh38
NC_000010.10:g.89720846_89720864delinsGCCAACCGATACTTTTCTC , CM000672.1:g.89720846_89720864delinsGCCAACCGATACTTTTCTC GRCh37
NC_000010.9:g.89710826_89710844delinsGCCAACCGATACTTTTCTC NCBI36
NG_007466.2:g.102651_102669delinsGCCAACCGATACTTTTCTC , LRG_311:g.102651_102669delinsGCCAACCGATACTTTTCTC

Transcript Alleles

HGVS Amino-acid change
ENST00000700029.2:c.1090_1108delinsGCCAACCGATACTTTTCTC ENSP00000514759.2:p.Ala364=
ENST00000710265.1:c.997_1015delinsGCCAACCGATACTTTTCTC ENSP00000518161.1:p.Ala333=
ENST00000472832.3:c.997_1015delinsGCCAACCGATACTTTTCTC ENSP00000483066.2:p.Ala333=
ENST00000688158.2:n.1732_1750delinsGCCAACCGATACTTTTCTC
ENST00000688922.2:c.*827_*845delinsGCCAACCGATACTTTTCTC ENSP00000508742.2:n.*827_*845delinsGCCAAC...
ENST00000700021.1:c.952_970delinsGCCAACCGATACTTTTCTC ENSP00000514757.1:p.Ala318=
ENST00000700022.1:c.*336_*354delinsGCCAACCGATACTTTTCTC ENSP00000514758.1:n.*336_*354delinsGCCAAC...
ENST00000700023.1:n.2155_2173delinsGCCAACCGATACTTTTCTC
ENST00000700024.1:n.2389_2407delinsGCCAACCGATACTTTTCTC
ENST00000700025.1:n.1766_1784delinsGCCAACCGATACTTTTCTC
ENST00000700026.1:n.634_652delinsGCCAACCGATACTTTTCTC
ENST00000706954.1:c.997_1015delinsGCCAACCGATACTTTTCTC ENSP00000516674.1:p.Ala333=
ENST00000706955.1:c.*1032_*1050delinsGCCAACCGATACTTTTCTC ENSP00000516675.1:n.*1032_*1050delinsGCCA...
ENST00000686459.1:c.*583_*601delinsGCCAACCGATACTTTTCTC ENSP00000508909.1:n.*583_*601delinsGCCAAC...
ENST00000688158.1:c.*1108_*1126delinsGCCAACCGATACTTTTCTC ENSP00000509254.1:n.*1108_*1126delinsGCCA...
ENST00000688308.1:c.997_1015delinsGCCAACCGATACTTTTCTC ENSP00000508752.1:p.Ala333=
ENST00000688922.1:c.918_936delinsGCCAACCGATACTTTTCTC
ENST00000693560.1:c.1516_1534delinsGCCAACCGATACTTTTCTC ENSP00000509861.1:p.Ala506=
ENST00000371953.8:c.997_1015delinsGCCAACCGATACTTTTCTC MANE Select ENSP00000361021.3:p.Ala333=
ENST00000371953.7:c.997_1015delinsGCCAACCGATACTTTTCTC ENSP00000361021.3:p.Ala333=
ENST00000472832.2:c.424_442delinsGCCAACCGATACTTTTCTC ENSP00000483066.1:p.Ala142=
NM_000314.5:c.997_1015delinsGCCAACCGATACTTTTCTC NP_000305.3:p.Ala333=
NM_000314.6:c.997_1015delinsGCCAACCGATACTTTTCTC NP_000305.3:p.Ala333=
NM_001304717.2:c.1516_1534delinsGCCAACCGATACTTTTCTC NP_001291646.2:p.Ala506=
NM_001304718.1:c.406_424delinsGCCAACCGATACTTTTCTC NP_001291647.1:p.Ala136=
XM_006717926.2:c.952_970delinsGCCAACCGATACTTTTCTC XP_006717989.1:p.Ala318=
XM_011539981.1:c.997_1015delinsGCCAACCGATACTTTTCTC XP_011538283.1:p.Ala333=
XM_011539982.1:c.901_919delinsGCCAACCGATACTTTTCTC XP_011538284.1:p.Ala301=
XR_945791.1:n.1567_1585delinsGCCAACCGATACTTTTCTC
NM_000314.7:c.997_1015delinsGCCAACCGATACTTTTCTC NP_000305.3:p.Ala333=
NM_001304717.5:c.1516_1534delinsGCCAACCGATACTTTTCTC NP_001291646.4:p.Ala506=
NM_001304718.2:c.406_424delinsGCCAACCGATACTTTTCTC NP_001291647.1:p.Ala136=
NM_000314.8:c.997_1015delinsGCCAACCGATACTTTTCTC MANE Select NP_000305.3:p.Ala333=