Canonical Allele Identifier: CA891841638
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965413_87965414delinsCG , CM000672.2:g.87965413_87965414delinsCG GRCh38
NC_000010.10:g.89725170_89725171delinsCG , CM000672.1:g.89725170_89725171delinsCG GRCh37
NC_000010.9:g.89715150_89715151delinsCG NCBI36
NG_007466.2:g.106975_106976delinsCG , LRG_311:g.106975_106976delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1246_1247delinsCG ENSP00000514759.2:p.Ser416Arg
ENST00000710265.1:c.*182_*183delinsCG ENSP00000518161.1:n.*182_*183delinsCG
ENST00000688158.2:n.1888_1889delinsCG
ENST00000688922.2:c.*983_*984delinsCG ENSP00000508742.2:n.*983_*984delinsCG
ENST00000700021.1:c.1108_1109delinsCG ENSP00000514757.1:p.Ser370Arg
ENST00000700022.1:c.*492_*493delinsCG ENSP00000514758.1:n.*492_*493delinsCG
ENST00000700023.1:n.2311_2312delinsCG
ENST00000700024.1:n.2545_2546delinsCG
ENST00000706954.1:c.1153_1154delinsCG ENSP00000516674.1:p.Ser385Arg
ENST00000706955.1:c.*1188_*1189delinsCG ENSP00000516675.1:n.*1188_*1189delinsCG
ENST00000686459.1:c.*739_*740delinsCG ENSP00000508909.1:n.*739_*740delinsCG
ENST00000688158.1:c.*1264_*1265delinsCG ENSP00000509254.1:n.*1264_*1265delinsCG
ENST00000688308.1:c.1153_1154delinsCG ENSP00000508752.1:p.Ser385Arg
ENST00000688922.1:c.1074_1075delinsCG
ENST00000693560.1:c.1672_1673delinsCG ENSP00000509861.1:p.Ser558Arg
ENST00000371953.8:c.1153_1154delinsCG MANE Select ENSP00000361021.3:p.Ser385Arg
ENST00000371953.7:c.1153_1154delinsCG ENSP00000361021.3:p.Ser385Arg
NM_000314.5:c.1153_1154delinsCG NP_000305.3:p.Ser385Arg
NM_000314.6:c.1153_1154delinsCG NP_000305.3:p.Ser385Arg
NM_001304717.2:c.1672_1673delinsCG NP_001291646.2:p.Ser558Arg
NM_001304718.1:c.562_563delinsCG NP_001291647.1:p.Ser188Arg
XM_006717926.2:c.1108_1109delinsCG XP_006717989.1:p.Ser370Arg
XM_011539982.1:c.1057_1058delinsCG XP_011538284.1:p.Ser353Arg
XR_945791.1:n.1723_1724delinsCG
NM_000314.7:c.1153_1154delinsCG NP_000305.3:p.Ser385Arg
NM_001304717.5:c.1672_1673delinsCG NP_001291646.4:p.Ser558Arg
NM_001304718.2:c.562_563delinsCG NP_001291647.1:p.Ser188Arg
NM_000314.8:c.1153_1154delinsCG MANE Select NP_000305.3:p.Ser385Arg