Canonical Allele Identifier: CA891837948
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965413_87965415delinsCCA , CM000672.2:g.87965413_87965415delinsCCA GRCh38
NC_000010.10:g.89725170_89725172delinsCCA , CM000672.1:g.89725170_89725172delinsCCA GRCh37
NC_000010.9:g.89715150_89715152delinsCCA NCBI36
NG_007466.2:g.106975_106977delinsCCA , LRG_311:g.106975_106977delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1246_1248delinsCCA ENSP00000514759.2:p.Ser416Pro
ENST00000710265.1:c.*182_*184delinsCCA ENSP00000518161.1:n.*182_*184delinsCCA
ENST00000688158.2:n.1888_1890delinsCCA
ENST00000688922.2:c.*983_*985delinsCCA ENSP00000508742.2:n.*983_*985delinsCCA
ENST00000700021.1:c.1108_1110delinsCCA ENSP00000514757.1:p.Ser370Pro
ENST00000700022.1:c.*492_*494delinsCCA ENSP00000514758.1:n.*492_*494delinsCCA
ENST00000700023.1:n.2311_2313delinsCCA
ENST00000700024.1:n.2545_2547delinsCCA
ENST00000706954.1:c.1153_1155delinsCCA ENSP00000516674.1:p.Ser385Pro
ENST00000706955.1:c.*1188_*1190delinsCCA ENSP00000516675.1:n.*1188_*1190delinsCCA
ENST00000686459.1:c.*739_*741delinsCCA ENSP00000508909.1:n.*739_*741delinsCCA
ENST00000688158.1:c.*1264_*1266delinsCCA ENSP00000509254.1:n.*1264_*1266delinsCCA
ENST00000688308.1:c.1153_1155delinsCCA ENSP00000508752.1:p.Ser385Pro
ENST00000688922.1:c.1074_1076delinsCCA
ENST00000693560.1:c.1672_1674delinsCCA ENSP00000509861.1:p.Ser558Pro
ENST00000371953.8:c.1153_1155delinsCCA MANE Select ENSP00000361021.3:p.Ser385Pro
ENST00000371953.7:c.1153_1155delinsCCA ENSP00000361021.3:p.Ser385Pro
NM_000314.5:c.1153_1155delinsCCA NP_000305.3:p.Ser385Pro
NM_000314.6:c.1153_1155delinsCCA NP_000305.3:p.Ser385Pro
NM_001304717.2:c.1672_1674delinsCCA NP_001291646.2:p.Ser558Pro
NM_001304718.1:c.562_564delinsCCA NP_001291647.1:p.Ser188Pro
XM_006717926.2:c.1108_1110delinsCCA XP_006717989.1:p.Ser370Pro
XM_011539982.1:c.1057_1059delinsCCA XP_011538284.1:p.Ser353Pro
XR_945791.1:n.1723_1725delinsCCA
NM_000314.7:c.1153_1155delinsCCA NP_000305.3:p.Ser385Pro
NM_001304717.5:c.1672_1674delinsCCA NP_001291646.4:p.Ser558Pro
NM_001304718.2:c.562_564delinsCCA NP_001291647.1:p.Ser188Pro
NM_000314.8:c.1153_1155delinsCCA MANE Select NP_000305.3:p.Ser385Pro