Canonical Allele Identifier: CA891837950

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965413_87965415delinsCAA , CM000672.2:g.87965413_87965415delinsCAA	GRCh38
NC_000010.10:g.89725170_89725172delinsCAA , CM000672.1:g.89725170_89725172delinsCAA	GRCh37
NC_000010.9:g.89715150_89715152delinsCAA	NCBI36
NG_007466.2:g.106975_106977delinsCAA , LRG_311:g.106975_106977delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1246_1248delinsCAA	ENSP00000514759.2:p.Ser416Gln
ENST00000710265.1:c.*182_*184delinsCAA	ENSP00000518161.1:n.*182_*184delinsCAA
ENST00000688158.2:n.1888_1890delinsCAA
ENST00000688922.2:c.*983_*985delinsCAA	ENSP00000508742.2:n.*983_*985delinsCAA
ENST00000700021.1:c.1108_1110delinsCAA	ENSP00000514757.1:p.Ser370Gln
ENST00000700022.1:c.*492_*494delinsCAA	ENSP00000514758.1:n.*492_*494delinsCAA
ENST00000700023.1:n.2311_2313delinsCAA
ENST00000700024.1:n.2545_2547delinsCAA
ENST00000706954.1:c.1153_1155delinsCAA	ENSP00000516674.1:p.Ser385Gln
ENST00000706955.1:c.*1188_*1190delinsCAA	ENSP00000516675.1:n.*1188_*1190delinsCAA
ENST00000686459.1:c.*739_*741delinsCAA	ENSP00000508909.1:n.*739_*741delinsCAA
ENST00000688158.1:c.*1264_*1266delinsCAA	ENSP00000509254.1:n.*1264_*1266delinsCAA
ENST00000688308.1:c.1153_1155delinsCAA	ENSP00000508752.1:p.Ser385Gln
ENST00000688922.1:c.1074_1076delinsCAA
ENST00000693560.1:c.1672_1674delinsCAA	ENSP00000509861.1:p.Ser558Gln
ENST00000371953.8:c.1153_1155delinsCAA MANE Select	ENSP00000361021.3:p.Ser385Gln
ENST00000371953.7:c.1153_1155delinsCAA	ENSP00000361021.3:p.Ser385Gln
NM_000314.5:c.1153_1155delinsCAA	NP_000305.3:p.Ser385Gln
NM_000314.6:c.1153_1155delinsCAA	NP_000305.3:p.Ser385Gln
NM_001304717.2:c.1672_1674delinsCAA	NP_001291646.2:p.Ser558Gln
NM_001304718.1:c.562_564delinsCAA	NP_001291647.1:p.Ser188Gln
XM_006717926.2:c.1108_1110delinsCAA	XP_006717989.1:p.Ser370Gln
XM_011539982.1:c.1057_1059delinsCAA	XP_011538284.1:p.Ser353Gln
XR_945791.1:n.1723_1725delinsCAA
NM_000314.7:c.1153_1155delinsCAA	NP_000305.3:p.Ser385Gln
NM_001304717.5:c.1672_1674delinsCAA	NP_001291646.4:p.Ser558Gln
NM_001304718.2:c.562_564delinsCAA	NP_001291647.1:p.Ser188Gln
NM_000314.8:c.1153_1155delinsCAA MANE Select	NP_000305.3:p.Ser385Gln