Canonical Allele Identifier: CA891837184
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965323_87965325delinsGCT , CM000672.2:g.87965323_87965325delinsGCT GRCh38
NC_000010.10:g.89725080_89725082delinsGCT , CM000672.1:g.89725080_89725082delinsGCT GRCh37
NC_000010.9:g.89715060_89715062delinsGCT NCBI36
NG_007466.2:g.106885_106887delinsGCT , LRG_311:g.106885_106887delinsGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1156_1158delinsGCT ENSP00000514759.2:p.Ser386Ala
ENST00000710265.1:c.*92_*94delinsGCT ENSP00000518161.1:n.*92_*94delinsGCT
ENST00000688158.2:n.1798_1800delinsGCT
ENST00000688922.2:c.*893_*895delinsGCT ENSP00000508742.2:n.*893_*895delinsGCT
ENST00000700021.1:c.1018_1020delinsGCT ENSP00000514757.1:p.Ser340Ala
ENST00000700022.1:c.*402_*404delinsGCT ENSP00000514758.1:n.*402_*404delinsGCT
ENST00000700023.1:n.2221_2223delinsGCT
ENST00000700024.1:n.2455_2457delinsGCT
ENST00000706954.1:c.1063_1065delinsGCT ENSP00000516674.1:p.Ser355Ala
ENST00000706955.1:c.*1098_*1100delinsGCT ENSP00000516675.1:n.*1098_*1100delinsGCT
ENST00000686459.1:c.*649_*651delinsGCT ENSP00000508909.1:n.*649_*651delinsGCT
ENST00000688158.1:c.*1174_*1176delinsGCT ENSP00000509254.1:n.*1174_*1176delinsGCT
ENST00000688308.1:c.1063_1065delinsGCT ENSP00000508752.1:p.Ser355Ala
ENST00000688922.1:c.984_986delinsGCT
ENST00000693560.1:c.1582_1584delinsGCT ENSP00000509861.1:p.Ser528Ala
ENST00000371953.8:c.1063_1065delinsGCT MANE Select ENSP00000361021.3:p.Ser355Ala
ENST00000371953.7:c.1063_1065delinsGCT ENSP00000361021.3:p.Ser355Ala
NM_000314.5:c.1063_1065delinsGCT NP_000305.3:p.Ser355Ala
NM_000314.6:c.1063_1065delinsGCT NP_000305.3:p.Ser355Ala
NM_001304717.2:c.1582_1584delinsGCT NP_001291646.2:p.Ser528Ala
NM_001304718.1:c.472_474delinsGCT NP_001291647.1:p.Ser158Ala
XM_006717926.2:c.1018_1020delinsGCT XP_006717989.1:p.Ser340Ala
XM_011539982.1:c.967_969delinsGCT XP_011538284.1:p.Ser323Ala
XR_945791.1:n.1633_1635delinsGCT
NM_000314.7:c.1063_1065delinsGCT NP_000305.3:p.Ser355Ala
NM_001304717.5:c.1582_1584delinsGCT NP_001291646.4:p.Ser528Ala
NM_001304718.2:c.472_474delinsGCT NP_001291647.1:p.Ser158Ala
NM_000314.8:c.1063_1065delinsGCT MANE Select NP_000305.3:p.Ser355Ala