Canonical Allele Identifier: CA2579926466
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965405_87965406delinsGA , CM000672.2:g.87965405_87965406delinsGA GRCh38
NC_000010.10:g.89725162_89725163delinsGA , CM000672.1:g.89725162_89725163delinsGA GRCh37
NC_000010.9:g.89715142_89715143delinsGA NCBI36
NG_007466.2:g.106967_106968delinsGA , LRG_311:g.106967_106968delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1238_1239delinsGA ENSP00000514759.2:p.Thr413Arg
ENST00000710265.1:c.*174_*175delinsGA ENSP00000518161.1:n.*174_*175delinsGA
ENST00000688158.2:n.1880_1881delinsGA
ENST00000688922.2:c.*975_*976delinsGA ENSP00000508742.2:n.*975_*976delinsGA
ENST00000700021.1:c.1100_1101delinsGA ENSP00000514757.1:p.Thr367Arg
ENST00000700022.1:c.*484_*485delinsGA ENSP00000514758.1:n.*484_*485delinsGA
ENST00000700023.1:n.2303_2304delinsGA
ENST00000700024.1:n.2537_2538delinsGA
ENST00000706954.1:c.1145_1146delinsGA ENSP00000516674.1:p.Thr382Arg
ENST00000706955.1:c.*1180_*1181delinsGA ENSP00000516675.1:n.*1180_*1181delinsGA
ENST00000686459.1:c.*731_*732delinsGA ENSP00000508909.1:n.*731_*732delinsGA
ENST00000688158.1:c.*1256_*1257delinsGA ENSP00000509254.1:n.*1256_*1257delinsGA
ENST00000688308.1:c.1145_1146delinsGA ENSP00000508752.1:p.Thr382Arg
ENST00000688922.1:c.1066_1067delinsGA
ENST00000693560.1:c.1664_1665delinsGA ENSP00000509861.1:p.Thr555Arg
ENST00000371953.8:c.1145_1146delinsGA MANE Select ENSP00000361021.3:p.Thr382Arg
ENST00000371953.7:c.1145_1146delinsGA ENSP00000361021.3:p.Thr382Arg
NM_000314.5:c.1145_1146delinsGA NP_000305.3:p.Thr382Arg
NM_000314.6:c.1145_1146delinsGA NP_000305.3:p.Thr382Arg
NM_001304717.2:c.1664_1665delinsGA NP_001291646.2:p.Thr555Arg
NM_001304718.1:c.554_555delinsGA NP_001291647.1:p.Thr185Arg
XM_006717926.2:c.1100_1101delinsGA XP_006717989.1:p.Thr367Arg
XM_011539982.1:c.1049_1050delinsGA XP_011538284.1:p.Thr350Arg
XR_945791.1:n.1715_1716delinsGA
NM_000314.7:c.1145_1146delinsGA NP_000305.3:p.Thr382Arg
NM_001304717.5:c.1664_1665delinsGA NP_001291646.4:p.Thr555Arg
NM_001304718.2:c.554_555delinsGA NP_001291647.1:p.Thr185Arg
NM_000314.8:c.1145_1146delinsGA MANE Select NP_000305.3:p.Thr382Arg