Canonical Allele Identifier: CA891836759

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961068_87961070delinsTAT , CM000672.2:g.87961068_87961070delinsTAT	GRCh38
NC_000010.10:g.89720825_89720827delinsTAT , CM000672.1:g.89720825_89720827delinsTAT	GRCh37
NC_000010.9:g.89710805_89710807delinsTAT	NCBI36
NG_007466.2:g.102630_102632delinsTAT , LRG_311:g.102630_102632delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1069_1071delinsTAT	ENSP00000514759.2:p.Asp357Tyr
ENST00000710265.1:c.976_978delinsTAT	ENSP00000518161.1:p.Asp326Tyr
ENST00000472832.3:c.976_978delinsTAT	ENSP00000483066.2:p.Asp326Tyr
ENST00000688158.2:n.1711_1713delinsTAT
ENST00000688922.2:c.*806_*808delinsTAT	ENSP00000508742.2:n.*806_*808delinsTAT
ENST00000700021.1:c.931_933delinsTAT	ENSP00000514757.1:p.Asp311Tyr
ENST00000700022.1:c.*315_*317delinsTAT	ENSP00000514758.1:n.*315_*317delinsTAT
ENST00000700023.1:n.2134_2136delinsTAT
ENST00000700024.1:n.2368_2370delinsTAT
ENST00000700025.1:n.1745_1747delinsTAT
ENST00000700026.1:n.613_615delinsTAT
ENST00000706954.1:c.976_978delinsTAT	ENSP00000516674.1:p.Asp326Tyr
ENST00000706955.1:c.*1011_*1013delinsTAT	ENSP00000516675.1:n.*1011_*1013delinsTAT
ENST00000686459.1:c.*562_*564delinsTAT	ENSP00000508909.1:n.*562_*564delinsTAT
ENST00000688158.1:c.*1087_*1089delinsTAT	ENSP00000509254.1:n.*1087_*1089delinsTAT
ENST00000688308.1:c.976_978delinsTAT	ENSP00000508752.1:p.Asp326Tyr
ENST00000688922.1:c.897_899delinsTAT
ENST00000693560.1:c.1495_1497delinsTAT	ENSP00000509861.1:p.Asp499Tyr
ENST00000371953.8:c.976_978delinsTAT MANE Select	ENSP00000361021.3:p.Asp326Tyr
ENST00000371953.7:c.976_978delinsTAT	ENSP00000361021.3:p.Asp326Tyr
ENST00000472832.2:c.403_405delinsTAT	ENSP00000483066.1:p.Asp135Tyr
NM_000314.5:c.976_978delinsTAT	NP_000305.3:p.Asp326Tyr
NM_000314.6:c.976_978delinsTAT	NP_000305.3:p.Asp326Tyr
NM_001304717.2:c.1495_1497delinsTAT	NP_001291646.2:p.Asp499Tyr
NM_001304718.1:c.385_387delinsTAT	NP_001291647.1:p.Asp129Tyr
XM_006717926.2:c.931_933delinsTAT	XP_006717989.1:p.Asp311Tyr
XM_011539981.1:c.976_978delinsTAT	XP_011538283.1:p.Asp326Tyr
XM_011539982.1:c.880_882delinsTAT	XP_011538284.1:p.Asp294Tyr
XR_945791.1:n.1546_1548delinsTAT
NM_000314.7:c.976_978delinsTAT	NP_000305.3:p.Asp326Tyr
NM_001304717.5:c.1495_1497delinsTAT	NP_001291646.4:p.Asp499Tyr
NM_001304718.2:c.385_387delinsTAT	NP_001291647.1:p.Asp129Tyr
NM_000314.8:c.976_978delinsTAT MANE Select	NP_000305.3:p.Asp326Tyr