Canonical Allele Identifier: CA891837548
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965365_87965367delinsAGA , CM000672.2:g.87965365_87965367delinsAGA GRCh38
NC_000010.10:g.89725122_89725124delinsAGA , CM000672.1:g.89725122_89725124delinsAGA GRCh37
NC_000010.9:g.89715102_89715104delinsAGA NCBI36
NG_007466.2:g.106927_106929delinsAGA , LRG_311:g.106927_106929delinsAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1198_1200delinsAGA ENSP00000514759.2:p.Val400Arg
ENST00000710265.1:c.*134_*136delinsAGA ENSP00000518161.1:n.*134_*136delinsAGA
ENST00000688158.2:n.1840_1842delinsAGA
ENST00000688922.2:c.*935_*937delinsAGA ENSP00000508742.2:n.*935_*937delinsAGA
ENST00000700021.1:c.1060_1062delinsAGA ENSP00000514757.1:p.Val354Arg
ENST00000700022.1:c.*444_*446delinsAGA ENSP00000514758.1:n.*444_*446delinsAGA
ENST00000700023.1:n.2263_2265delinsAGA
ENST00000700024.1:n.2497_2499delinsAGA
ENST00000706954.1:c.1105_1107delinsAGA ENSP00000516674.1:p.Val369Arg
ENST00000706955.1:c.*1140_*1142delinsAGA ENSP00000516675.1:n.*1140_*1142delinsAGA
ENST00000686459.1:c.*691_*693delinsAGA ENSP00000508909.1:n.*691_*693delinsAGA
ENST00000688158.1:c.*1216_*1218delinsAGA ENSP00000509254.1:n.*1216_*1218delinsAGA
ENST00000688308.1:c.1105_1107delinsAGA ENSP00000508752.1:p.Val369Arg
ENST00000688922.1:c.1026_1028delinsAGA
ENST00000693560.1:c.1624_1626delinsAGA ENSP00000509861.1:p.Val542Arg
ENST00000371953.8:c.1105_1107delinsAGA MANE Select ENSP00000361021.3:p.Val369Arg
ENST00000371953.7:c.1105_1107delinsAGA ENSP00000361021.3:p.Val369Arg
NM_000314.5:c.1105_1107delinsAGA NP_000305.3:p.Val369Arg
NM_000314.6:c.1105_1107delinsAGA NP_000305.3:p.Val369Arg
NM_001304717.2:c.1624_1626delinsAGA NP_001291646.2:p.Val542Arg
NM_001304718.1:c.514_516delinsAGA NP_001291647.1:p.Val172Arg
XM_006717926.2:c.1060_1062delinsAGA XP_006717989.1:p.Val354Arg
XM_011539982.1:c.1009_1011delinsAGA XP_011538284.1:p.Val337Arg
XR_945791.1:n.1675_1677delinsAGA
NM_000314.7:c.1105_1107delinsAGA NP_000305.3:p.Val369Arg
NM_001304717.5:c.1624_1626delinsAGA NP_001291646.4:p.Val542Arg
NM_001304718.2:c.514_516delinsAGA NP_001291647.1:p.Val172Arg
NM_000314.8:c.1105_1107delinsAGA MANE Select NP_000305.3:p.Val369Arg