Canonical Allele Identifier: CA891841252

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961026_87961027delinsCG , CM000672.2:g.87961026_87961027delinsCG	GRCh38
NC_000010.10:g.89720783_89720784delinsCG , CM000672.1:g.89720783_89720784delinsCG	GRCh37
NC_000010.9:g.89710763_89710764delinsCG	NCBI36
NG_007466.2:g.102588_102589delinsCG , LRG_311:g.102588_102589delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1027_1028delinsCG	ENSP00000514759.2:p.Asp343Arg
ENST00000710265.1:c.934_935delinsCG	ENSP00000518161.1:p.Asp312Arg
ENST00000472832.3:c.934_935delinsCG	ENSP00000483066.2:p.Asp312Arg
ENST00000688158.2:n.1669_1670delinsCG
ENST00000688922.2:c.*764_*765delinsCG	ENSP00000508742.2:n.*764_*765delinsCG
ENST00000700021.1:c.889_890delinsCG	ENSP00000514757.1:p.Asp297Arg
ENST00000700022.1:c.*273_*274delinsCG	ENSP00000514758.1:n.*273_*274delinsCG
ENST00000700023.1:n.2092_2093delinsCG
ENST00000700024.1:n.2326_2327delinsCG
ENST00000700025.1:n.1703_1704delinsCG
ENST00000700026.1:n.571_572delinsCG
ENST00000706954.1:c.934_935delinsCG	ENSP00000516674.1:p.Asp312Arg
ENST00000706955.1:c.*969_*970delinsCG	ENSP00000516675.1:n.*969_*970delinsCG
ENST00000686459.1:c.*520_*521delinsCG	ENSP00000508909.1:n.*520_*521delinsCG
ENST00000688158.1:c.*1045_*1046delinsCG	ENSP00000509254.1:n.*1045_*1046delinsCG
ENST00000688308.1:c.934_935delinsCG	ENSP00000508752.1:p.Asp312Arg
ENST00000688922.1:c.855_856delinsCG
ENST00000693560.1:c.1453_1454delinsCG	ENSP00000509861.1:p.Asp485Arg
ENST00000371953.8:c.934_935delinsCG MANE Select	ENSP00000361021.3:p.Asp312Arg
ENST00000371953.7:c.934_935delinsCG	ENSP00000361021.3:p.Asp312Arg
ENST00000472832.2:c.361_362delinsCG	ENSP00000483066.1:p.Asp121Arg
NM_000314.5:c.934_935delinsCG	NP_000305.3:p.Asp312Arg
NM_000314.6:c.934_935delinsCG	NP_000305.3:p.Asp312Arg
NM_001304717.2:c.1453_1454delinsCG	NP_001291646.2:p.Asp485Arg
NM_001304718.1:c.343_344delinsCG	NP_001291647.1:p.Asp115Arg
XM_006717926.2:c.889_890delinsCG	XP_006717989.1:p.Asp297Arg
XM_011539981.1:c.934_935delinsCG	XP_011538283.1:p.Asp312Arg
XM_011539982.1:c.838_839delinsCG	XP_011538284.1:p.Asp280Arg
XR_945791.1:n.1504_1505delinsCG
NM_000314.7:c.934_935delinsCG	NP_000305.3:p.Asp312Arg
NM_001304717.5:c.1453_1454delinsCG	NP_001291646.4:p.Asp485Arg
NM_001304718.2:c.343_344delinsCG	NP_001291647.1:p.Asp115Arg
NM_000314.8:c.934_935delinsCG MANE Select	NP_000305.3:p.Asp312Arg