Canonical Allele Identifier: CA2579926434

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965452_87965454delinsGTT , CM000672.2:g.87965452_87965454delinsGTT	GRCh38
NC_000010.10:g.89725209_89725211delinsGTT , CM000672.1:g.89725209_89725211delinsGTT	GRCh37
NC_000010.9:g.89715189_89715191delinsGTT	NCBI36
NG_007466.2:g.107014_107016delinsGTT , LRG_311:g.107014_107016delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1285_1287delinsGTT	ENSP00000514759.2:p.Thr429Val
ENST00000710265.1:c.*221_*223delinsGTT	ENSP00000518161.1:n.*221_*223delinsGTT
ENST00000688158.2:n.1927_1929delinsGTT
ENST00000688922.2:c.*1022_*1024delinsGTT	ENSP00000508742.2:n.*1022_*1024delinsGTT
ENST00000700021.1:c.1147_1149delinsGTT	ENSP00000514757.1:p.Thr383Val
ENST00000700022.1:c.*531_*533delinsGTT	ENSP00000514758.1:n.*531_*533delinsGTT
ENST00000700023.1:n.2350_2352delinsGTT
ENST00000700024.1:n.2584_2586delinsGTT
ENST00000706954.1:c.1192_1194delinsGTT	ENSP00000516674.1:p.Thr398Val
ENST00000706955.1:c.*1227_*1229delinsGTT	ENSP00000516675.1:n.*1227_*1229delinsGTT
ENST00000686459.1:c.*778_*780delinsGTT	ENSP00000508909.1:n.*778_*780delinsGTT
ENST00000688158.1:c.*1303_*1305delinsGTT	ENSP00000509254.1:n.*1303_*1305delinsGTT
ENST00000688308.1:c.1192_1194delinsGTT	ENSP00000508752.1:p.Thr398Val
ENST00000688922.1:c.1113_1115delinsGTT
ENST00000693560.1:c.1711_1713delinsGTT	ENSP00000509861.1:p.Thr571Val
ENST00000371953.8:c.1192_1194delinsGTT MANE Select	ENSP00000361021.3:p.Thr398Val
ENST00000371953.7:c.1192_1194delinsGTT	ENSP00000361021.3:p.Thr398Val
NM_000314.5:c.1192_1194delinsGTT	NP_000305.3:p.Thr398Val
NM_000314.6:c.1192_1194delinsGTT	NP_000305.3:p.Thr398Val
NM_001304717.2:c.1711_1713delinsGTT	NP_001291646.2:p.Thr571Val
NM_001304718.1:c.601_603delinsGTT	NP_001291647.1:p.Thr201Val
XM_006717926.2:c.1147_1149delinsGTT	XP_006717989.1:p.Thr383Val
XM_011539982.1:c.1096_1098delinsGTT	XP_011538284.1:p.Thr366Val
XR_945791.1:n.1762_1764delinsGTT
NM_000314.7:c.1192_1194delinsGTT	NP_000305.3:p.Thr398Val
NM_001304717.5:c.1711_1713delinsGTT	NP_001291646.4:p.Thr571Val
NM_001304718.2:c.601_603delinsGTT	NP_001291647.1:p.Thr201Val
NM_000314.8:c.1192_1194delinsGTT MANE Select	NP_000305.3:p.Thr398Val