Canonical Allele Identifier: CA2579926446

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965347_87965349delinsTTG , CM000672.2:g.87965347_87965349delinsTTG	GRCh38
NC_000010.10:g.89725104_89725106delinsTTG , CM000672.1:g.89725104_89725106delinsTTG	GRCh37
NC_000010.9:g.89715084_89715086delinsTTG	NCBI36
NG_007466.2:g.106909_106911delinsTTG , LRG_311:g.106909_106911delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1180_1182delinsTTG	ENSP00000514759.2:p.Thr394Leu
ENST00000710265.1:c.*116_*118delinsTTG	ENSP00000518161.1:n.*116_*118delinsTTG
ENST00000688158.2:n.1822_1824delinsTTG
ENST00000688922.2:c.*917_*919delinsTTG	ENSP00000508742.2:n.*917_*919delinsTTG
ENST00000700021.1:c.1042_1044delinsTTG	ENSP00000514757.1:p.Thr348Leu
ENST00000700022.1:c.*426_*428delinsTTG	ENSP00000514758.1:n.*426_*428delinsTTG
ENST00000700023.1:n.2245_2247delinsTTG
ENST00000700024.1:n.2479_2481delinsTTG
ENST00000706954.1:c.1087_1089delinsTTG	ENSP00000516674.1:p.Thr363Leu
ENST00000706955.1:c.*1122_*1124delinsTTG	ENSP00000516675.1:n.*1122_*1124delinsTTG
ENST00000686459.1:c.*673_*675delinsTTG	ENSP00000508909.1:n.*673_*675delinsTTG
ENST00000688158.1:c.*1198_*1200delinsTTG	ENSP00000509254.1:n.*1198_*1200delinsTTG
ENST00000688308.1:c.1087_1089delinsTTG	ENSP00000508752.1:p.Thr363Leu
ENST00000688922.1:c.1008_1010delinsTTG
ENST00000693560.1:c.1606_1608delinsTTG	ENSP00000509861.1:p.Thr536Leu
ENST00000371953.8:c.1087_1089delinsTTG MANE Select	ENSP00000361021.3:p.Thr363Leu
ENST00000371953.7:c.1087_1089delinsTTG	ENSP00000361021.3:p.Thr363Leu
NM_000314.5:c.1087_1089delinsTTG	NP_000305.3:p.Thr363Leu
NM_000314.6:c.1087_1089delinsTTG	NP_000305.3:p.Thr363Leu
NM_001304717.2:c.1606_1608delinsTTG	NP_001291646.2:p.Thr536Leu
NM_001304718.1:c.496_498delinsTTG	NP_001291647.1:p.Thr166Leu
XM_006717926.2:c.1042_1044delinsTTG	XP_006717989.1:p.Thr348Leu
XM_011539982.1:c.991_993delinsTTG	XP_011538284.1:p.Thr331Leu
XR_945791.1:n.1657_1659delinsTTG
NM_000314.7:c.1087_1089delinsTTG	NP_000305.3:p.Thr363Leu
NM_001304717.5:c.1606_1608delinsTTG	NP_001291646.4:p.Thr536Leu
NM_001304718.2:c.496_498delinsTTG	NP_001291647.1:p.Thr166Leu
NM_000314.8:c.1087_1089delinsTTG MANE Select	NP_000305.3:p.Thr363Leu