Canonical Allele Identifier: CA891836993

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933090_87933092delinsAGA , CM000672.2:g.87933090_87933092delinsAGA	GRCh38
NC_000010.10:g.89692847_89692849delinsAGA , CM000672.1:g.89692847_89692849delinsAGA	GRCh37
NC_000010.9:g.89682827_89682829delinsAGA	NCBI36
NG_007466.2:g.74652_74654delinsAGA , LRG_311:g.74652_74654delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.331_333delinsAGA	ENSP00000514759.2:p.Trp111Arg
ENST00000710265.1:c.331_333delinsAGA	ENSP00000518161.1:p.Trp111Arg
ENST00000472832.3:c.331_333delinsAGA	ENSP00000483066.2:p.Trp111Arg
ENST00000688158.2:n.1066_1068delinsAGA
ENST00000688922.2:c.*161_*163delinsAGA	ENSP00000508742.2:n.*161_*163delinsAGA
ENST00000700021.1:c.286_288delinsAGA	ENSP00000514757.1:p.Trp96Arg
ENST00000700022.1:c.331_333delinsAGA	ENSP00000514758.1:p.Trp111Arg
ENST00000700029.1:c.165_167delinsAGA
ENST00000706954.1:c.331_333delinsAGA	ENSP00000516674.1:p.Trp111Arg
ENST00000706955.1:c.*366_*368delinsAGA	ENSP00000516675.1:n.*366_*368delinsAGA
ENST00000686459.1:c.331_333delinsAGA	ENSP00000508909.1:p.Trp111Arg
ENST00000688158.1:c.*442_*444delinsAGA	ENSP00000509254.1:n.*442_*444delinsAGA
ENST00000688308.1:c.331_333delinsAGA	ENSP00000508752.1:p.Trp111Arg
ENST00000688922.1:c.252_254delinsAGA
ENST00000693560.1:c.850_852delinsAGA	ENSP00000509861.1:p.Trp284Arg
ENST00000371953.8:c.331_333delinsAGA MANE Select	ENSP00000361021.3:p.Trp111Arg
ENST00000371953.7:c.331_333delinsAGA	ENSP00000361021.3:p.Trp111Arg
ENST00000498703.1:n.157_159delinsAGA
ENST00000610634.1:c.229_231delinsAGA	ENSP00000477517.1:p.Trp77Arg
NM_000314.5:c.331_333delinsAGA	NP_000305.3:p.Trp111Arg
NM_000314.6:c.331_333delinsAGA	NP_000305.3:p.Trp111Arg
NM_001304717.2:c.850_852delinsAGA	NP_001291646.2:p.Trp284Arg
NM_001304718.1:c.-420_-418delinsAGA	NP_001291647.1:n.-420_-418delinsAGA
XM_006717926.2:c.286_288delinsAGA	XP_006717989.1:p.Trp96Arg
XM_011539981.1:c.331_333delinsAGA	XP_011538283.1:p.Trp111Arg
XM_011539982.1:c.235_237delinsAGA	XP_011538284.1:p.Trp79Arg
XR_945789.1:n.1043_1045delinsAGA
XR_945790.1:n.1043_1045delinsAGA
XR_945791.1:n.1043_1045delinsAGA
NM_000314.7:c.331_333delinsAGA	NP_000305.3:p.Trp111Arg
NM_001304717.5:c.850_852delinsAGA	NP_001291646.4:p.Trp284Arg
NM_001304718.2:c.-420_-418delinsAGA	NP_001291647.1:n.-420_-418delinsAGA
NM_000314.8:c.331_333delinsAGA MANE Select	NP_000305.3:p.Trp111Arg