Canonical Allele Identifier: CA891837946
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965413_87965414delinsCA , CM000672.2:g.87965413_87965414delinsCA GRCh38
NC_000010.10:g.89725170_89725171delinsCA , CM000672.1:g.89725170_89725171delinsCA GRCh37
NC_000010.9:g.89715150_89715151delinsCA NCBI36
NG_007466.2:g.106975_106976delinsCA , LRG_311:g.106975_106976delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1246_1247delinsCA ENSP00000514759.2:p.Ser416His
ENST00000710265.1:c.*182_*183delinsCA ENSP00000518161.1:n.*182_*183delinsCA
ENST00000688158.2:n.1888_1889delinsCA
ENST00000688922.2:c.*983_*984delinsCA ENSP00000508742.2:n.*983_*984delinsCA
ENST00000700021.1:c.1108_1109delinsCA ENSP00000514757.1:p.Ser370His
ENST00000700022.1:c.*492_*493delinsCA ENSP00000514758.1:n.*492_*493delinsCA
ENST00000700023.1:n.2311_2312delinsCA
ENST00000700024.1:n.2545_2546delinsCA
ENST00000706954.1:c.1153_1154delinsCA ENSP00000516674.1:p.Ser385His
ENST00000706955.1:c.*1188_*1189delinsCA ENSP00000516675.1:n.*1188_*1189delinsCA
ENST00000686459.1:c.*739_*740delinsCA ENSP00000508909.1:n.*739_*740delinsCA
ENST00000688158.1:c.*1264_*1265delinsCA ENSP00000509254.1:n.*1264_*1265delinsCA
ENST00000688308.1:c.1153_1154delinsCA ENSP00000508752.1:p.Ser385His
ENST00000688922.1:c.1074_1075delinsCA
ENST00000693560.1:c.1672_1673delinsCA ENSP00000509861.1:p.Ser558His
ENST00000371953.8:c.1153_1154delinsCA MANE Select ENSP00000361021.3:p.Ser385His
ENST00000371953.7:c.1153_1154delinsCA ENSP00000361021.3:p.Ser385His
NM_000314.5:c.1153_1154delinsCA NP_000305.3:p.Ser385His
NM_000314.6:c.1153_1154delinsCA NP_000305.3:p.Ser385His
NM_001304717.2:c.1672_1673delinsCA NP_001291646.2:p.Ser558His
NM_001304718.1:c.562_563delinsCA NP_001291647.1:p.Ser188His
XM_006717926.2:c.1108_1109delinsCA XP_006717989.1:p.Ser370His
XM_011539982.1:c.1057_1058delinsCA XP_011538284.1:p.Ser353His
XR_945791.1:n.1723_1724delinsCA
NM_000314.7:c.1153_1154delinsCA NP_000305.3:p.Ser385His
NM_001304717.5:c.1672_1673delinsCA NP_001291646.4:p.Ser558His
NM_001304718.2:c.562_563delinsCA NP_001291647.1:p.Ser188His
NM_000314.8:c.1153_1154delinsCA MANE Select NP_000305.3:p.Ser385His