Canonical Allele Identifier: CA891837937

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965410_87965412delinsTAT , CM000672.2:g.87965410_87965412delinsTAT	GRCh38
NC_000010.10:g.89725167_89725169delinsTAT , CM000672.1:g.89725167_89725169delinsTAT	GRCh37
NC_000010.9:g.89715147_89715149delinsTAT	NCBI36
NG_007466.2:g.106972_106974delinsTAT , LRG_311:g.106972_106974delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1243_1245delinsTAT	ENSP00000514759.2:p.Asp415Tyr
ENST00000710265.1:c.*179_*181delinsTAT	ENSP00000518161.1:n.*179_*181delinsTAT
ENST00000688158.2:n.1885_1887delinsTAT
ENST00000688922.2:c.*980_*982delinsTAT	ENSP00000508742.2:n.*980_*982delinsTAT
ENST00000700021.1:c.1105_1107delinsTAT	ENSP00000514757.1:p.Asp369Tyr
ENST00000700022.1:c.*489_*491delinsTAT	ENSP00000514758.1:n.*489_*491delinsTAT
ENST00000700023.1:n.2308_2310delinsTAT
ENST00000700024.1:n.2542_2544delinsTAT
ENST00000706954.1:c.1150_1152delinsTAT	ENSP00000516674.1:p.Asp384Tyr
ENST00000706955.1:c.*1185_*1187delinsTAT	ENSP00000516675.1:n.*1185_*1187delinsTAT
ENST00000686459.1:c.*736_*738delinsTAT	ENSP00000508909.1:n.*736_*738delinsTAT
ENST00000688158.1:c.*1261_*1263delinsTAT	ENSP00000509254.1:n.*1261_*1263delinsTAT
ENST00000688308.1:c.1150_1152delinsTAT	ENSP00000508752.1:p.Asp384Tyr
ENST00000688922.1:c.1071_1073delinsTAT
ENST00000693560.1:c.1669_1671delinsTAT	ENSP00000509861.1:p.Asp557Tyr
ENST00000371953.8:c.1150_1152delinsTAT MANE Select	ENSP00000361021.3:p.Asp384Tyr
ENST00000371953.7:c.1150_1152delinsTAT	ENSP00000361021.3:p.Asp384Tyr
NM_000314.5:c.1150_1152delinsTAT	NP_000305.3:p.Asp384Tyr
NM_000314.6:c.1150_1152delinsTAT	NP_000305.3:p.Asp384Tyr
NM_001304717.2:c.1669_1671delinsTAT	NP_001291646.2:p.Asp557Tyr
NM_001304718.1:c.559_561delinsTAT	NP_001291647.1:p.Asp187Tyr
XM_006717926.2:c.1105_1107delinsTAT	XP_006717989.1:p.Asp369Tyr
XM_011539982.1:c.1054_1056delinsTAT	XP_011538284.1:p.Asp352Tyr
XR_945791.1:n.1720_1722delinsTAT
NM_000314.7:c.1150_1152delinsTAT	NP_000305.3:p.Asp384Tyr
NM_001304717.5:c.1669_1671delinsTAT	NP_001291646.4:p.Asp557Tyr
NM_001304718.2:c.559_561delinsTAT	NP_001291647.1:p.Asp187Tyr
NM_000314.8:c.1150_1152delinsTAT MANE Select	NP_000305.3:p.Asp384Tyr