Canonical Allele Identifier: CA891841700

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965452_87965453delinsGT , CM000672.2:g.87965452_87965453delinsGT	GRCh38
NC_000010.10:g.89725209_89725210delinsGT , CM000672.1:g.89725209_89725210delinsGT	GRCh37
NC_000010.9:g.89715189_89715190delinsGT	NCBI36
NG_007466.2:g.107014_107015delinsGT , LRG_311:g.107014_107015delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1285_1286delinsGT	ENSP00000514759.2:p.Thr429Val
ENST00000710265.1:c.*221_*222delinsGT	ENSP00000518161.1:n.*221_*222delinsGT
ENST00000688158.2:n.1927_1928delinsGT
ENST00000688922.2:c.*1022_*1023delinsGT	ENSP00000508742.2:n.*1022_*1023delinsGT
ENST00000700021.1:c.1147_1148delinsGT	ENSP00000514757.1:p.Thr383Val
ENST00000700022.1:c.*531_*532delinsGT	ENSP00000514758.1:n.*531_*532delinsGT
ENST00000700023.1:n.2350_2351delinsGT
ENST00000700024.1:n.2584_2585delinsGT
ENST00000706954.1:c.1192_1193delinsGT	ENSP00000516674.1:p.Thr398Val
ENST00000706955.1:c.*1227_*1228delinsGT	ENSP00000516675.1:n.*1227_*1228delinsGT
ENST00000686459.1:c.*778_*779delinsGT	ENSP00000508909.1:n.*778_*779delinsGT
ENST00000688158.1:c.*1303_*1304delinsGT	ENSP00000509254.1:n.*1303_*1304delinsGT
ENST00000688308.1:c.1192_1193delinsGT	ENSP00000508752.1:p.Thr398Val
ENST00000688922.1:c.1113_1114delinsGT
ENST00000693560.1:c.1711_1712delinsGT	ENSP00000509861.1:p.Thr571Val
ENST00000371953.8:c.1192_1193delinsGT MANE Select	ENSP00000361021.3:p.Thr398Val
ENST00000371953.7:c.1192_1193delinsGT	ENSP00000361021.3:p.Thr398Val
NM_000314.5:c.1192_1193delinsGT	NP_000305.3:p.Thr398Val
NM_000314.6:c.1192_1193delinsGT	NP_000305.3:p.Thr398Val
NM_001304717.2:c.1711_1712delinsGT	NP_001291646.2:p.Thr571Val
NM_001304718.1:c.601_602delinsGT	NP_001291647.1:p.Thr201Val
XM_006717926.2:c.1147_1148delinsGT	XP_006717989.1:p.Thr383Val
XM_011539982.1:c.1096_1097delinsGT	XP_011538284.1:p.Thr366Val
XR_945791.1:n.1762_1763delinsGT
NM_000314.7:c.1192_1193delinsGT	NP_000305.3:p.Thr398Val
NM_001304717.5:c.1711_1712delinsGT	NP_001291646.4:p.Thr571Val
NM_001304718.2:c.601_602delinsGT	NP_001291647.1:p.Thr201Val
NM_000314.8:c.1192_1193delinsGT MANE Select	NP_000305.3:p.Thr398Val