Canonical Allele Identifier: CA891836204

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961020_87961022delinsAGA , CM000672.2:g.87961020_87961022delinsAGA	GRCh38
NC_000010.10:g.89720777_89720779delinsAGA , CM000672.1:g.89720777_89720779delinsAGA	GRCh37
NC_000010.9:g.89710757_89710759delinsAGA	NCBI36
NG_007466.2:g.102582_102584delinsAGA , LRG_311:g.102582_102584delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1021_1023delinsAGA	ENSP00000514759.2:p.Asp341Arg
ENST00000710265.1:c.928_930delinsAGA	ENSP00000518161.1:p.Asp310Arg
ENST00000472832.3:c.928_930delinsAGA	ENSP00000483066.2:p.Asp310Arg
ENST00000688158.2:n.1663_1665delinsAGA
ENST00000688922.2:c.*758_*760delinsAGA	ENSP00000508742.2:n.*758_*760delinsAGA
ENST00000700021.1:c.883_885delinsAGA	ENSP00000514757.1:p.Asp295Arg
ENST00000700022.1:c.*267_*269delinsAGA	ENSP00000514758.1:n.*267_*269delinsAGA
ENST00000700023.1:n.2086_2088delinsAGA
ENST00000700024.1:n.2320_2322delinsAGA
ENST00000700025.1:n.1697_1699delinsAGA
ENST00000700026.1:n.565_567delinsAGA
ENST00000706954.1:c.928_930delinsAGA	ENSP00000516674.1:p.Asp310Arg
ENST00000706955.1:c.*963_*965delinsAGA	ENSP00000516675.1:n.*963_*965delinsAGA
ENST00000686459.1:c.*514_*516delinsAGA	ENSP00000508909.1:n.*514_*516delinsAGA
ENST00000688158.1:c.*1039_*1041delinsAGA	ENSP00000509254.1:n.*1039_*1041delinsAGA
ENST00000688308.1:c.928_930delinsAGA	ENSP00000508752.1:p.Asp310Arg
ENST00000688922.1:c.849_851delinsAGA
ENST00000693560.1:c.1447_1449delinsAGA	ENSP00000509861.1:p.Asp483Arg
ENST00000371953.8:c.928_930delinsAGA MANE Select	ENSP00000361021.3:p.Asp310Arg
ENST00000371953.7:c.928_930delinsAGA	ENSP00000361021.3:p.Asp310Arg
ENST00000472832.2:c.355_357delinsAGA	ENSP00000483066.1:p.Asp119Arg
NM_000314.5:c.928_930delinsAGA	NP_000305.3:p.Asp310Arg
NM_000314.6:c.928_930delinsAGA	NP_000305.3:p.Asp310Arg
NM_001304717.2:c.1447_1449delinsAGA	NP_001291646.2:p.Asp483Arg
NM_001304718.1:c.337_339delinsAGA	NP_001291647.1:p.Asp113Arg
XM_006717926.2:c.883_885delinsAGA	XP_006717989.1:p.Asp295Arg
XM_011539981.1:c.928_930delinsAGA	XP_011538283.1:p.Asp310Arg
XM_011539982.1:c.832_834delinsAGA	XP_011538284.1:p.Asp278Arg
XR_945791.1:n.1498_1500delinsAGA
NM_000314.7:c.928_930delinsAGA	NP_000305.3:p.Asp310Arg
NM_001304717.5:c.1447_1449delinsAGA	NP_001291646.4:p.Asp483Arg
NM_001304718.2:c.337_339delinsAGA	NP_001291647.1:p.Asp113Arg
NM_000314.8:c.928_930delinsAGA MANE Select	NP_000305.3:p.Asp310Arg