Canonical Allele Identifier: CA891837944
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87965413_87965414delinsAA , CM000672.2:g.87965413_87965414delinsAA GRCh38
NC_000010.10:g.89725170_89725171delinsAA , CM000672.1:g.89725170_89725171delinsAA GRCh37
NC_000010.9:g.89715150_89715151delinsAA NCBI36
NG_007466.2:g.106975_106976delinsAA , LRG_311:g.106975_106976delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1246_1247delinsAA ENSP00000514759.2:p.Ser416Asn
ENST00000710265.1:c.*182_*183delinsAA ENSP00000518161.1:n.*182_*183delinsAA
ENST00000688158.2:n.1888_1889delinsAA
ENST00000688922.2:c.*983_*984delinsAA ENSP00000508742.2:n.*983_*984delinsAA
ENST00000700021.1:c.1108_1109delinsAA ENSP00000514757.1:p.Ser370Asn
ENST00000700022.1:c.*492_*493delinsAA ENSP00000514758.1:n.*492_*493delinsAA
ENST00000700023.1:n.2311_2312delinsAA
ENST00000700024.1:n.2545_2546delinsAA
ENST00000706954.1:c.1153_1154delinsAA ENSP00000516674.1:p.Ser385Asn
ENST00000706955.1:c.*1188_*1189delinsAA ENSP00000516675.1:n.*1188_*1189delinsAA
ENST00000686459.1:c.*739_*740delinsAA ENSP00000508909.1:n.*739_*740delinsAA
ENST00000688158.1:c.*1264_*1265delinsAA ENSP00000509254.1:n.*1264_*1265delinsAA
ENST00000688308.1:c.1153_1154delinsAA ENSP00000508752.1:p.Ser385Asn
ENST00000688922.1:c.1074_1075delinsAA
ENST00000693560.1:c.1672_1673delinsAA ENSP00000509861.1:p.Ser558Asn
ENST00000371953.8:c.1153_1154delinsAA MANE Select ENSP00000361021.3:p.Ser385Asn
ENST00000371953.7:c.1153_1154delinsAA ENSP00000361021.3:p.Ser385Asn
NM_000314.5:c.1153_1154delinsAA NP_000305.3:p.Ser385Asn
NM_000314.6:c.1153_1154delinsAA NP_000305.3:p.Ser385Asn
NM_001304717.2:c.1672_1673delinsAA NP_001291646.2:p.Ser558Asn
NM_001304718.1:c.562_563delinsAA NP_001291647.1:p.Ser188Asn
XM_006717926.2:c.1108_1109delinsAA XP_006717989.1:p.Ser370Asn
XM_011539982.1:c.1057_1058delinsAA XP_011538284.1:p.Ser353Asn
XR_945791.1:n.1723_1724delinsAA
NM_000314.7:c.1153_1154delinsAA NP_000305.3:p.Ser385Asn
NM_001304717.5:c.1672_1673delinsAA NP_001291646.4:p.Ser558Asn
NM_001304718.2:c.562_563delinsAA NP_001291647.1:p.Ser188Asn
NM_000314.8:c.1153_1154delinsAA MANE Select NP_000305.3:p.Ser385Asn