Canonical Allele Identifier: CA891837087

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965314_87965315delinsAT , CM000672.2:g.87965314_87965315delinsAT	GRCh38
NC_000010.10:g.89725071_89725072delinsAT , CM000672.1:g.89725071_89725072delinsAT	GRCh37
NC_000010.9:g.89715051_89715052delinsAT	NCBI36
NG_007466.2:g.106876_106877delinsAT , LRG_311:g.106876_106877delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1147_1148delinsAT	ENSP00000514759.2:p.Glu383Met
ENST00000710265.1:c.*83_*84delinsAT	ENSP00000518161.1:n.*83_*84delinsAT
ENST00000688158.2:n.1789_1790delinsAT
ENST00000688922.2:c.*884_*885delinsAT	ENSP00000508742.2:n.*884_*885delinsAT
ENST00000700021.1:c.1009_1010delinsAT	ENSP00000514757.1:p.Glu337Met
ENST00000700022.1:c.*393_*394delinsAT	ENSP00000514758.1:n.*393_*394delinsAT
ENST00000700023.1:n.2212_2213delinsAT
ENST00000700024.1:n.2446_2447delinsAT
ENST00000706954.1:c.1054_1055delinsAT	ENSP00000516674.1:p.Glu352Met
ENST00000706955.1:c.*1089_*1090delinsAT	ENSP00000516675.1:n.*1089_*1090delinsAT
ENST00000686459.1:c.*640_*641delinsAT	ENSP00000508909.1:n.*640_*641delinsAT
ENST00000688158.1:c.*1165_*1166delinsAT	ENSP00000509254.1:n.*1165_*1166delinsAT
ENST00000688308.1:c.1054_1055delinsAT	ENSP00000508752.1:p.Glu352Met
ENST00000688922.1:c.975_976delinsAT
ENST00000693560.1:c.1573_1574delinsAT	ENSP00000509861.1:p.Glu525Met
ENST00000371953.8:c.1054_1055delinsAT MANE Select	ENSP00000361021.3:p.Glu352Met
ENST00000371953.7:c.1054_1055delinsAT	ENSP00000361021.3:p.Glu352Met
NM_000314.5:c.1054_1055delinsAT	NP_000305.3:p.Glu352Met
NM_000314.6:c.1054_1055delinsAT	NP_000305.3:p.Glu352Met
NM_001304717.2:c.1573_1574delinsAT	NP_001291646.2:p.Glu525Met
NM_001304718.1:c.463_464delinsAT	NP_001291647.1:p.Glu155Met
XM_006717926.2:c.1009_1010delinsAT	XP_006717989.1:p.Glu337Met
XM_011539982.1:c.958_959delinsAT	XP_011538284.1:p.Glu320Met
XR_945791.1:n.1624_1625delinsAT
NM_000314.7:c.1054_1055delinsAT	NP_000305.3:p.Glu352Met
NM_001304717.5:c.1573_1574delinsAT	NP_001291646.4:p.Glu525Met
NM_001304718.2:c.463_464delinsAT	NP_001291647.1:p.Glu155Met
NM_000314.8:c.1054_1055delinsAT MANE Select	NP_000305.3:p.Glu352Met