Canonical Allele Identifier: CA891837947

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965413_87965415delinsAGA , CM000672.2:g.87965413_87965415delinsAGA	GRCh38
NC_000010.10:g.89725170_89725172delinsAGA , CM000672.1:g.89725170_89725172delinsAGA	GRCh37
NC_000010.9:g.89715150_89715152delinsAGA	NCBI36
NG_007466.2:g.106975_106977delinsAGA , LRG_311:g.106975_106977delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1246_1248delinsAGA	ENSP00000514759.2:p.Ser416Arg
ENST00000710265.1:c.*182_*184delinsAGA	ENSP00000518161.1:n.*182_*184delinsAGA
ENST00000688158.2:n.1888_1890delinsAGA
ENST00000688922.2:c.*983_*985delinsAGA	ENSP00000508742.2:n.*983_*985delinsAGA
ENST00000700021.1:c.1108_1110delinsAGA	ENSP00000514757.1:p.Ser370Arg
ENST00000700022.1:c.*492_*494delinsAGA	ENSP00000514758.1:n.*492_*494delinsAGA
ENST00000700023.1:n.2311_2313delinsAGA
ENST00000700024.1:n.2545_2547delinsAGA
ENST00000706954.1:c.1153_1155delinsAGA	ENSP00000516674.1:p.Ser385Arg
ENST00000706955.1:c.*1188_*1190delinsAGA	ENSP00000516675.1:n.*1188_*1190delinsAGA
ENST00000686459.1:c.*739_*741delinsAGA	ENSP00000508909.1:n.*739_*741delinsAGA
ENST00000688158.1:c.*1264_*1266delinsAGA	ENSP00000509254.1:n.*1264_*1266delinsAGA
ENST00000688308.1:c.1153_1155delinsAGA	ENSP00000508752.1:p.Ser385Arg
ENST00000688922.1:c.1074_1076delinsAGA
ENST00000693560.1:c.1672_1674delinsAGA	ENSP00000509861.1:p.Ser558Arg
ENST00000371953.8:c.1153_1155delinsAGA MANE Select	ENSP00000361021.3:p.Ser385Arg
ENST00000371953.7:c.1153_1155delinsAGA	ENSP00000361021.3:p.Ser385Arg
NM_000314.5:c.1153_1155delinsAGA	NP_000305.3:p.Ser385Arg
NM_000314.6:c.1153_1155delinsAGA	NP_000305.3:p.Ser385Arg
NM_001304717.2:c.1672_1674delinsAGA	NP_001291646.2:p.Ser558Arg
NM_001304718.1:c.562_564delinsAGA	NP_001291647.1:p.Ser188Arg
XM_006717926.2:c.1108_1110delinsAGA	XP_006717989.1:p.Ser370Arg
XM_011539982.1:c.1057_1059delinsAGA	XP_011538284.1:p.Ser353Arg
XR_945791.1:n.1723_1725delinsAGA
NM_000314.7:c.1153_1155delinsAGA	NP_000305.3:p.Ser385Arg
NM_001304717.5:c.1672_1674delinsAGA	NP_001291646.4:p.Ser558Arg
NM_001304718.2:c.562_564delinsAGA	NP_001291647.1:p.Ser188Arg
NM_000314.8:c.1153_1155delinsAGA MANE Select	NP_000305.3:p.Ser385Arg