Canonical Allele Identifier: CA891837427

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965348_87965349delinsGA , CM000672.2:g.87965348_87965349delinsGA	GRCh38
NC_000010.10:g.89725105_89725106delinsGA , CM000672.1:g.89725105_89725106delinsGA	GRCh37
NC_000010.9:g.89715085_89715086delinsGA	NCBI36
NG_007466.2:g.106910_106911delinsGA , LRG_311:g.106910_106911delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1181_1182delinsGA	ENSP00000514759.2:p.Thr394Arg
ENST00000710265.1:c.*117_*118delinsGA	ENSP00000518161.1:n.*117_*118delinsGA
ENST00000688158.2:n.1823_1824delinsGA
ENST00000688922.2:c.*918_*919delinsGA	ENSP00000508742.2:n.*918_*919delinsGA
ENST00000700021.1:c.1043_1044delinsGA	ENSP00000514757.1:p.Thr348Arg
ENST00000700022.1:c.*427_*428delinsGA	ENSP00000514758.1:n.*427_*428delinsGA
ENST00000700023.1:n.2246_2247delinsGA
ENST00000700024.1:n.2480_2481delinsGA
ENST00000706954.1:c.1088_1089delinsGA	ENSP00000516674.1:p.Thr363Arg
ENST00000706955.1:c.*1123_*1124delinsGA	ENSP00000516675.1:n.*1123_*1124delinsGA
ENST00000686459.1:c.*674_*675delinsGA	ENSP00000508909.1:n.*674_*675delinsGA
ENST00000688158.1:c.*1199_*1200delinsGA	ENSP00000509254.1:n.*1199_*1200delinsGA
ENST00000688308.1:c.1088_1089delinsGA	ENSP00000508752.1:p.Thr363Arg
ENST00000688922.1:c.1009_1010delinsGA
ENST00000693560.1:c.1607_1608delinsGA	ENSP00000509861.1:p.Thr536Arg
ENST00000371953.8:c.1088_1089delinsGA MANE Select	ENSP00000361021.3:p.Thr363Arg
ENST00000371953.7:c.1088_1089delinsGA	ENSP00000361021.3:p.Thr363Arg
NM_000314.5:c.1088_1089delinsGA	NP_000305.3:p.Thr363Arg
NM_000314.6:c.1088_1089delinsGA	NP_000305.3:p.Thr363Arg
NM_001304717.2:c.1607_1608delinsGA	NP_001291646.2:p.Thr536Arg
NM_001304718.1:c.497_498delinsGA	NP_001291647.1:p.Thr166Arg
XM_006717926.2:c.1043_1044delinsGA	XP_006717989.1:p.Thr348Arg
XM_011539982.1:c.992_993delinsGA	XP_011538284.1:p.Thr331Arg
XR_945791.1:n.1658_1659delinsGA
NM_000314.7:c.1088_1089delinsGA	NP_000305.3:p.Thr363Arg
NM_001304717.5:c.1607_1608delinsGA	NP_001291646.4:p.Thr536Arg
NM_001304718.2:c.497_498delinsGA	NP_001291647.1:p.Thr166Arg
NM_000314.8:c.1088_1089delinsGA MANE Select	NP_000305.3:p.Thr363Arg