Canonical Allele Identifier: CA2579926626

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961095_87961097delinsTAT , CM000672.2:g.87961095_87961097delinsTAT	GRCh38
NC_000010.10:g.89720852_89720854delinsTAT , CM000672.1:g.89720852_89720854delinsTAT	GRCh37
NC_000010.9:g.89710832_89710834delinsTAT	NCBI36
NG_007466.2:g.102657_102659delinsTAT , LRG_311:g.102657_102659delinsTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1096_1098delinsTAT	ENSP00000514759.2:p.Arg366Tyr
ENST00000710265.1:c.1003_1005delinsTAT	ENSP00000518161.1:p.Arg335Tyr
ENST00000472832.3:c.1003_1005delinsTAT	ENSP00000483066.2:p.Arg335Tyr
ENST00000688158.2:n.1738_1740delinsTAT
ENST00000688922.2:c.*833_*835delinsTAT	ENSP00000508742.2:n.*833_*835delinsTAT
ENST00000700021.1:c.958_960delinsTAT	ENSP00000514757.1:p.Arg320Tyr
ENST00000700022.1:c.*342_*344delinsTAT	ENSP00000514758.1:n.*342_*344delinsTAT
ENST00000700023.1:n.2161_2163delinsTAT
ENST00000700024.1:n.2395_2397delinsTAT
ENST00000700025.1:n.1772_1774delinsTAT
ENST00000700026.1:n.640_642delinsTAT
ENST00000706954.1:c.1003_1005delinsTAT	ENSP00000516674.1:p.Arg335Tyr
ENST00000706955.1:c.*1038_*1040delinsTAT	ENSP00000516675.1:n.*1038_*1040delinsTAT
ENST00000686459.1:c.*589_*591delinsTAT	ENSP00000508909.1:n.*589_*591delinsTAT
ENST00000688158.1:c.*1114_*1116delinsTAT	ENSP00000509254.1:n.*1114_*1116delinsTAT
ENST00000688308.1:c.1003_1005delinsTAT	ENSP00000508752.1:p.Arg335Tyr
ENST00000688922.1:c.924_926delinsTAT
ENST00000693560.1:c.1522_1524delinsTAT	ENSP00000509861.1:p.Arg508Tyr
ENST00000371953.8:c.1003_1005delinsTAT MANE Select	ENSP00000361021.3:p.Arg335Tyr
ENST00000371953.7:c.1003_1005delinsTAT	ENSP00000361021.3:p.Arg335Tyr
ENST00000472832.2:c.430_432delinsTAT	ENSP00000483066.1:p.Arg144Tyr
NM_000314.5:c.1003_1005delinsTAT	NP_000305.3:p.Arg335Tyr
NM_000314.6:c.1003_1005delinsTAT	NP_000305.3:p.Arg335Tyr
NM_001304717.2:c.1522_1524delinsTAT	NP_001291646.2:p.Arg508Tyr
NM_001304718.1:c.412_414delinsTAT	NP_001291647.1:p.Arg138Tyr
XM_006717926.2:c.958_960delinsTAT	XP_006717989.1:p.Arg320Tyr
XM_011539981.1:c.1003_1005delinsTAT	XP_011538283.1:p.Arg335Tyr
XM_011539982.1:c.907_909delinsTAT	XP_011538284.1:p.Arg303Tyr
XR_945791.1:n.1573_1575delinsTAT
NM_000314.7:c.1003_1005delinsTAT	NP_000305.3:p.Arg335Tyr
NM_001304717.5:c.1522_1524delinsTAT	NP_001291646.4:p.Arg508Tyr
NM_001304718.2:c.412_414delinsTAT	NP_001291647.1:p.Arg138Tyr
NM_000314.8:c.1003_1005delinsTAT MANE Select	NP_000305.3:p.Arg335Tyr