Canonical Allele Identifier: CA891841642
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965414_87965415delinsGG , CM000672.2:g.87965414_87965415delinsGG GRCh38
NC_000010.10:g.89725171_89725172delinsGG , CM000672.1:g.89725171_89725172delinsGG GRCh37
NC_000010.9:g.89715151_89715152delinsGG NCBI36
NG_007466.2:g.106976_106977delinsGG , LRG_311:g.106976_106977delinsGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1247_1248delinsGG ENSP00000514759.2:p.Ser416Trp
ENST00000710265.1:c.*183_*184delinsGG ENSP00000518161.1:n.*183_*184delinsGG
ENST00000688158.2:n.1889_1890delinsGG
ENST00000688922.2:c.*984_*985delinsGG ENSP00000508742.2:n.*984_*985delinsGG
ENST00000700021.1:c.1109_1110delinsGG ENSP00000514757.1:p.Ser370Trp
ENST00000700022.1:c.*493_*494delinsGG ENSP00000514758.1:n.*493_*494delinsGG
ENST00000700023.1:n.2312_2313delinsGG
ENST00000700024.1:n.2546_2547delinsGG
ENST00000706954.1:c.1154_1155delinsGG ENSP00000516674.1:p.Ser385Trp
ENST00000706955.1:c.*1189_*1190delinsGG ENSP00000516675.1:n.*1189_*1190delinsGG
ENST00000686459.1:c.*740_*741delinsGG ENSP00000508909.1:n.*740_*741delinsGG
ENST00000688158.1:c.*1265_*1266delinsGG ENSP00000509254.1:n.*1265_*1266delinsGG
ENST00000688308.1:c.1154_1155delinsGG ENSP00000508752.1:p.Ser385Trp
ENST00000688922.1:c.1075_1076delinsGG
ENST00000693560.1:c.1673_1674delinsGG ENSP00000509861.1:p.Ser558Trp
ENST00000371953.8:c.1154_1155delinsGG MANE Select ENSP00000361021.3:p.Ser385Trp
ENST00000371953.7:c.1154_1155delinsGG ENSP00000361021.3:p.Ser385Trp
NM_000314.5:c.1154_1155delinsGG NP_000305.3:p.Ser385Trp
NM_000314.6:c.1154_1155delinsGG NP_000305.3:p.Ser385Trp
NM_001304717.2:c.1673_1674delinsGG NP_001291646.2:p.Ser558Trp
NM_001304718.1:c.563_564delinsGG NP_001291647.1:p.Ser188Trp
XM_006717926.2:c.1109_1110delinsGG XP_006717989.1:p.Ser370Trp
XM_011539982.1:c.1058_1059delinsGG XP_011538284.1:p.Ser353Trp
XR_945791.1:n.1724_1725delinsGG
NM_000314.7:c.1154_1155delinsGG NP_000305.3:p.Ser385Trp
NM_001304717.5:c.1673_1674delinsGG NP_001291646.4:p.Ser558Trp
NM_001304718.2:c.563_564delinsGG NP_001291647.1:p.Ser188Trp
NM_000314.8:c.1154_1155delinsGG MANE Select NP_000305.3:p.Ser385Trp