Canonical Allele Identifier: CA891841569
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965323_87965324delinsGG , CM000672.2:g.87965323_87965324delinsGG GRCh38
NC_000010.10:g.89725080_89725081delinsGG , CM000672.1:g.89725080_89725081delinsGG GRCh37
NC_000010.9:g.89715060_89715061delinsGG NCBI36
NG_007466.2:g.106885_106886delinsGG , LRG_311:g.106885_106886delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1156_1157delinsGG ENSP00000514759.2:p.Ser386Gly
ENST00000710265.1:c.*92_*93delinsGG ENSP00000518161.1:n.*92_*93delinsGG
ENST00000688158.2:n.1798_1799delinsGG
ENST00000688922.2:c.*893_*894delinsGG ENSP00000508742.2:n.*893_*894delinsGG
ENST00000700021.1:c.1018_1019delinsGG ENSP00000514757.1:p.Ser340Gly
ENST00000700022.1:c.*402_*403delinsGG ENSP00000514758.1:n.*402_*403delinsGG
ENST00000700023.1:n.2221_2222delinsGG
ENST00000700024.1:n.2455_2456delinsGG
ENST00000706954.1:c.1063_1064delinsGG ENSP00000516674.1:p.Ser355Gly
ENST00000706955.1:c.*1098_*1099delinsGG ENSP00000516675.1:n.*1098_*1099delinsGG
ENST00000686459.1:c.*649_*650delinsGG ENSP00000508909.1:n.*649_*650delinsGG
ENST00000688158.1:c.*1174_*1175delinsGG ENSP00000509254.1:n.*1174_*1175delinsGG
ENST00000688308.1:c.1063_1064delinsGG ENSP00000508752.1:p.Ser355Gly
ENST00000688922.1:c.984_985delinsGG
ENST00000693560.1:c.1582_1583delinsGG ENSP00000509861.1:p.Ser528Gly
ENST00000371953.8:c.1063_1064delinsGG MANE Select ENSP00000361021.3:p.Ser355Gly
ENST00000371953.7:c.1063_1064delinsGG ENSP00000361021.3:p.Ser355Gly
NM_000314.5:c.1063_1064delinsGG NP_000305.3:p.Ser355Gly
NM_000314.6:c.1063_1064delinsGG NP_000305.3:p.Ser355Gly
NM_001304717.2:c.1582_1583delinsGG NP_001291646.2:p.Ser528Gly
NM_001304718.1:c.472_473delinsGG NP_001291647.1:p.Ser158Gly
XM_006717926.2:c.1018_1019delinsGG XP_006717989.1:p.Ser340Gly
XM_011539982.1:c.967_968delinsGG XP_011538284.1:p.Ser323Gly
XR_945791.1:n.1633_1634delinsGG
NM_000314.7:c.1063_1064delinsGG NP_000305.3:p.Ser355Gly
NM_001304717.5:c.1582_1583delinsGG NP_001291646.4:p.Ser528Gly
NM_001304718.2:c.472_473delinsGG NP_001291647.1:p.Ser158Gly
NM_000314.8:c.1063_1064delinsGG MANE Select NP_000305.3:p.Ser355Gly