Canonical Allele Identifier: CA891841728
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965462_87965463delinsAT , CM000672.2:g.87965462_87965463delinsAT GRCh38
NC_000010.10:g.89725219_89725220delinsAT , CM000672.1:g.89725219_89725220delinsAT GRCh37
NC_000010.9:g.89715199_89715200delinsAT NCBI36
NG_007466.2:g.107024_107025delinsAT , LRG_311:g.107024_107025delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1295_1296delinsAT ENSP00000514759.2:p.Thr432Asn
ENST00000710265.1:c.*231_*232delinsAT ENSP00000518161.1:n.*231_*232delinsAT
ENST00000688158.2:n.1937_1938delinsAT
ENST00000688922.2:c.*1032_*1033delinsAT ENSP00000508742.2:n.*1032_*1033delinsAT
ENST00000700021.1:c.1157_1158delinsAT ENSP00000514757.1:p.Thr386Asn
ENST00000700022.1:c.*541_*542delinsAT ENSP00000514758.1:n.*541_*542delinsAT
ENST00000700023.1:n.2360_2361delinsAT
ENST00000700024.1:n.2594_2595delinsAT
ENST00000706954.1:c.1202_1203delinsAT ENSP00000516674.1:p.Thr401Asn
ENST00000706955.1:c.*1237_*1238delinsAT ENSP00000516675.1:n.*1237_*1238delinsAT
ENST00000686459.1:c.*788_*789delinsAT ENSP00000508909.1:n.*788_*789delinsAT
ENST00000688158.1:c.*1313_*1314delinsAT ENSP00000509254.1:n.*1313_*1314delinsAT
ENST00000688308.1:c.1202_1203delinsAT ENSP00000508752.1:p.Thr401Asn
ENST00000688922.1:c.1123_1124delinsAT
ENST00000693560.1:c.1721_1722delinsAT ENSP00000509861.1:p.Thr574Asn
ENST00000371953.8:c.1202_1203delinsAT MANE Select ENSP00000361021.3:p.Thr401Asn
ENST00000371953.7:c.1202_1203delinsAT ENSP00000361021.3:p.Thr401Asn
NM_000314.5:c.1202_1203delinsAT NP_000305.3:p.Thr401Asn
NM_000314.6:c.1202_1203delinsAT NP_000305.3:p.Thr401Asn
NM_001304717.2:c.1721_1722delinsAT NP_001291646.2:p.Thr574Asn
NM_001304718.1:c.611_612delinsAT NP_001291647.1:p.Thr204Asn
XM_006717926.2:c.1157_1158delinsAT XP_006717989.1:p.Thr386Asn
XM_011539982.1:c.1106_1107delinsAT XP_011538284.1:p.Thr369Asn
XR_945791.1:n.1772_1773delinsAT
NM_000314.7:c.1202_1203delinsAT NP_000305.3:p.Thr401Asn
NM_001304717.5:c.1721_1722delinsAT NP_001291646.4:p.Thr574Asn
NM_001304718.2:c.611_612delinsAT NP_001291647.1:p.Thr204Asn
NM_000314.8:c.1202_1203delinsAT MANE Select NP_000305.3:p.Thr401Asn