Canonical Allele Identifier: CA891837933

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965410_87965412delinsCAA , CM000672.2:g.87965410_87965412delinsCAA	GRCh38
NC_000010.10:g.89725167_89725169delinsCAA , CM000672.1:g.89725167_89725169delinsCAA	GRCh37
NC_000010.9:g.89715147_89715149delinsCAA	NCBI36
NG_007466.2:g.106972_106974delinsCAA , LRG_311:g.106972_106974delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1243_1245delinsCAA	ENSP00000514759.2:p.Asp415Gln
ENST00000710265.1:c.*179_*181delinsCAA	ENSP00000518161.1:n.*179_*181delinsCAA
ENST00000688158.2:n.1885_1887delinsCAA
ENST00000688922.2:c.*980_*982delinsCAA	ENSP00000508742.2:n.*980_*982delinsCAA
ENST00000700021.1:c.1105_1107delinsCAA	ENSP00000514757.1:p.Asp369Gln
ENST00000700022.1:c.*489_*491delinsCAA	ENSP00000514758.1:n.*489_*491delinsCAA
ENST00000700023.1:n.2308_2310delinsCAA
ENST00000700024.1:n.2542_2544delinsCAA
ENST00000706954.1:c.1150_1152delinsCAA	ENSP00000516674.1:p.Asp384Gln
ENST00000706955.1:c.*1185_*1187delinsCAA	ENSP00000516675.1:n.*1185_*1187delinsCAA
ENST00000686459.1:c.*736_*738delinsCAA	ENSP00000508909.1:n.*736_*738delinsCAA
ENST00000688158.1:c.*1261_*1263delinsCAA	ENSP00000509254.1:n.*1261_*1263delinsCAA
ENST00000688308.1:c.1150_1152delinsCAA	ENSP00000508752.1:p.Asp384Gln
ENST00000688922.1:c.1071_1073delinsCAA
ENST00000693560.1:c.1669_1671delinsCAA	ENSP00000509861.1:p.Asp557Gln
ENST00000371953.8:c.1150_1152delinsCAA MANE Select	ENSP00000361021.3:p.Asp384Gln
ENST00000371953.7:c.1150_1152delinsCAA	ENSP00000361021.3:p.Asp384Gln
NM_000314.5:c.1150_1152delinsCAA	NP_000305.3:p.Asp384Gln
NM_000314.6:c.1150_1152delinsCAA	NP_000305.3:p.Asp384Gln
NM_001304717.2:c.1669_1671delinsCAA	NP_001291646.2:p.Asp557Gln
NM_001304718.1:c.559_561delinsCAA	NP_001291647.1:p.Asp187Gln
XM_006717926.2:c.1105_1107delinsCAA	XP_006717989.1:p.Asp369Gln
XM_011539982.1:c.1054_1056delinsCAA	XP_011538284.1:p.Asp352Gln
XR_945791.1:n.1720_1722delinsCAA
NM_000314.7:c.1150_1152delinsCAA	NP_000305.3:p.Asp384Gln
NM_001304717.5:c.1669_1671delinsCAA	NP_001291646.4:p.Asp557Gln
NM_001304718.2:c.559_561delinsCAA	NP_001291647.1:p.Asp187Gln
NM_000314.8:c.1150_1152delinsCAA MANE Select	NP_000305.3:p.Asp384Gln