Canonical Allele Identifier: CA891838218

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965453_87965454delinsTT , CM000672.2:g.87965453_87965454delinsTT	GRCh38
NC_000010.10:g.89725210_89725211delinsTT , CM000672.1:g.89725210_89725211delinsTT	GRCh37
NC_000010.9:g.89715190_89715191delinsTT	NCBI36
NG_007466.2:g.107015_107016delinsTT , LRG_311:g.107015_107016delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1286_1287delinsTT	ENSP00000514759.2:p.Thr429Ile
ENST00000710265.1:c.*222_*223delinsTT	ENSP00000518161.1:n.*222_*223delinsTT
ENST00000688158.2:n.1928_1929delinsTT
ENST00000688922.2:c.*1023_*1024delinsTT	ENSP00000508742.2:n.*1023_*1024delinsTT
ENST00000700021.1:c.1148_1149delinsTT	ENSP00000514757.1:p.Thr383Ile
ENST00000700022.1:c.*532_*533delinsTT	ENSP00000514758.1:n.*532_*533delinsTT
ENST00000700023.1:n.2351_2352delinsTT
ENST00000700024.1:n.2585_2586delinsTT
ENST00000706954.1:c.1193_1194delinsTT	ENSP00000516674.1:p.Thr398Ile
ENST00000706955.1:c.*1228_*1229delinsTT	ENSP00000516675.1:n.*1228_*1229delinsTT
ENST00000686459.1:c.*779_*780delinsTT	ENSP00000508909.1:n.*779_*780delinsTT
ENST00000688158.1:c.*1304_*1305delinsTT	ENSP00000509254.1:n.*1304_*1305delinsTT
ENST00000688308.1:c.1193_1194delinsTT	ENSP00000508752.1:p.Thr398Ile
ENST00000688922.1:c.1114_1115delinsTT
ENST00000693560.1:c.1712_1713delinsTT	ENSP00000509861.1:p.Thr571Ile
ENST00000371953.8:c.1193_1194delinsTT MANE Select	ENSP00000361021.3:p.Thr398Ile
ENST00000371953.7:c.1193_1194delinsTT	ENSP00000361021.3:p.Thr398Ile
NM_000314.5:c.1193_1194delinsTT	NP_000305.3:p.Thr398Ile
NM_000314.6:c.1193_1194delinsTT	NP_000305.3:p.Thr398Ile
NM_001304717.2:c.1712_1713delinsTT	NP_001291646.2:p.Thr571Ile
NM_001304718.1:c.602_603delinsTT	NP_001291647.1:p.Thr201Ile
XM_006717926.2:c.1148_1149delinsTT	XP_006717989.1:p.Thr383Ile
XM_011539982.1:c.1097_1098delinsTT	XP_011538284.1:p.Thr366Ile
XR_945791.1:n.1763_1764delinsTT
NM_000314.7:c.1193_1194delinsTT	NP_000305.3:p.Thr398Ile
NM_001304717.5:c.1712_1713delinsTT	NP_001291646.4:p.Thr571Ile
NM_001304718.2:c.602_603delinsTT	NP_001291647.1:p.Thr201Ile
NM_000314.8:c.1193_1194delinsTT MANE Select	NP_000305.3:p.Thr398Ile