Canonical Allele Identifier: CA891836692

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961062_87961064delinsAGA , CM000672.2:g.87961062_87961064delinsAGA	GRCh38
NC_000010.10:g.89720819_89720821delinsAGA , CM000672.1:g.89720819_89720821delinsAGA	GRCh37
NC_000010.9:g.89710799_89710801delinsAGA	NCBI36
NG_007466.2:g.102624_102626delinsAGA , LRG_311:g.102624_102626delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1063_1065delinsAGA	ENSP00000514759.2:p.Asp355Arg
ENST00000710265.1:c.970_972delinsAGA	ENSP00000518161.1:p.Asp324Arg
ENST00000472832.3:c.970_972delinsAGA	ENSP00000483066.2:p.Asp324Arg
ENST00000688158.2:n.1705_1707delinsAGA
ENST00000688922.2:c.*800_*802delinsAGA	ENSP00000508742.2:n.*800_*802delinsAGA
ENST00000700021.1:c.925_927delinsAGA	ENSP00000514757.1:p.Asp309Arg
ENST00000700022.1:c.*309_*311delinsAGA	ENSP00000514758.1:n.*309_*311delinsAGA
ENST00000700023.1:n.2128_2130delinsAGA
ENST00000700024.1:n.2362_2364delinsAGA
ENST00000700025.1:n.1739_1741delinsAGA
ENST00000700026.1:n.607_609delinsAGA
ENST00000706954.1:c.970_972delinsAGA	ENSP00000516674.1:p.Asp324Arg
ENST00000706955.1:c.*1005_*1007delinsAGA	ENSP00000516675.1:n.*1005_*1007delinsAGA
ENST00000686459.1:c.*556_*558delinsAGA	ENSP00000508909.1:n.*556_*558delinsAGA
ENST00000688158.1:c.*1081_*1083delinsAGA	ENSP00000509254.1:n.*1081_*1083delinsAGA
ENST00000688308.1:c.970_972delinsAGA	ENSP00000508752.1:p.Asp324Arg
ENST00000688922.1:c.891_893delinsAGA
ENST00000693560.1:c.1489_1491delinsAGA	ENSP00000509861.1:p.Asp497Arg
ENST00000371953.8:c.970_972delinsAGA MANE Select	ENSP00000361021.3:p.Asp324Arg
ENST00000371953.7:c.970_972delinsAGA	ENSP00000361021.3:p.Asp324Arg
ENST00000472832.2:c.397_399delinsAGA	ENSP00000483066.1:p.Asp133Arg
NM_000314.5:c.970_972delinsAGA	NP_000305.3:p.Asp324Arg
NM_000314.6:c.970_972delinsAGA	NP_000305.3:p.Asp324Arg
NM_001304717.2:c.1489_1491delinsAGA	NP_001291646.2:p.Asp497Arg
NM_001304718.1:c.379_381delinsAGA	NP_001291647.1:p.Asp127Arg
XM_006717926.2:c.925_927delinsAGA	XP_006717989.1:p.Asp309Arg
XM_011539981.1:c.970_972delinsAGA	XP_011538283.1:p.Asp324Arg
XM_011539982.1:c.874_876delinsAGA	XP_011538284.1:p.Asp292Arg
XR_945791.1:n.1540_1542delinsAGA
NM_000314.7:c.970_972delinsAGA	NP_000305.3:p.Asp324Arg
NM_001304717.5:c.1489_1491delinsAGA	NP_001291646.4:p.Asp497Arg
NM_001304718.2:c.379_381delinsAGA	NP_001291647.1:p.Asp127Arg
NM_000314.8:c.970_972delinsAGA MANE Select	NP_000305.3:p.Asp324Arg