Canonical Allele Identifier: CA891837766

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965389_87965391delinsAGA , CM000672.2:g.87965389_87965391delinsAGA	GRCh38
NC_000010.10:g.89725146_89725148delinsAGA , CM000672.1:g.89725146_89725148delinsAGA	GRCh37
NC_000010.9:g.89715126_89715128delinsAGA	NCBI36
NG_007466.2:g.106951_106953delinsAGA , LRG_311:g.106951_106953delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1222_1224delinsAGA	ENSP00000514759.2:p.Tyr408Arg
ENST00000710265.1:c.*158_*160delinsAGA	ENSP00000518161.1:n.*158_*160delinsAGA
ENST00000688158.2:n.1864_1866delinsAGA
ENST00000688922.2:c.*959_*961delinsAGA	ENSP00000508742.2:n.*959_*961delinsAGA
ENST00000700021.1:c.1084_1086delinsAGA	ENSP00000514757.1:p.Tyr362Arg
ENST00000700022.1:c.*468_*470delinsAGA	ENSP00000514758.1:n.*468_*470delinsAGA
ENST00000700023.1:n.2287_2289delinsAGA
ENST00000700024.1:n.2521_2523delinsAGA
ENST00000706954.1:c.1129_1131delinsAGA	ENSP00000516674.1:p.Tyr377Arg
ENST00000706955.1:c.*1164_*1166delinsAGA	ENSP00000516675.1:n.*1164_*1166delinsAGA
ENST00000686459.1:c.*715_*717delinsAGA	ENSP00000508909.1:n.*715_*717delinsAGA
ENST00000688158.1:c.*1240_*1242delinsAGA	ENSP00000509254.1:n.*1240_*1242delinsAGA
ENST00000688308.1:c.1129_1131delinsAGA	ENSP00000508752.1:p.Tyr377Arg
ENST00000688922.1:c.1050_1052delinsAGA
ENST00000693560.1:c.1648_1650delinsAGA	ENSP00000509861.1:p.Tyr550Arg
ENST00000371953.8:c.1129_1131delinsAGA MANE Select	ENSP00000361021.3:p.Tyr377Arg
ENST00000371953.7:c.1129_1131delinsAGA	ENSP00000361021.3:p.Tyr377Arg
NM_000314.5:c.1129_1131delinsAGA	NP_000305.3:p.Tyr377Arg
NM_000314.6:c.1129_1131delinsAGA	NP_000305.3:p.Tyr377Arg
NM_001304717.2:c.1648_1650delinsAGA	NP_001291646.2:p.Tyr550Arg
NM_001304718.1:c.538_540delinsAGA	NP_001291647.1:p.Tyr180Arg
XM_006717926.2:c.1084_1086delinsAGA	XP_006717989.1:p.Tyr362Arg
XM_011539982.1:c.1033_1035delinsAGA	XP_011538284.1:p.Tyr345Arg
XR_945791.1:n.1699_1701delinsAGA
NM_000314.7:c.1129_1131delinsAGA	NP_000305.3:p.Tyr377Arg
NM_001304717.5:c.1648_1650delinsAGA	NP_001291646.4:p.Tyr550Arg
NM_001304718.2:c.538_540delinsAGA	NP_001291647.1:p.Tyr180Arg
NM_000314.8:c.1129_1131delinsAGA MANE Select	NP_000305.3:p.Tyr377Arg