Canonical Allele Identifier: CA891838063

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965429_87965430delinsCT , CM000672.2:g.87965429_87965430delinsCT	GRCh38
NC_000010.10:g.89725186_89725187delinsCT , CM000672.1:g.89725186_89725187delinsCT	GRCh37
NC_000010.9:g.89715166_89715167delinsCT	NCBI36
NG_007466.2:g.106991_106992delinsCT , LRG_311:g.106991_106992delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1262_1263delinsCT	ENSP00000514759.2:p.Glu421Ala
ENST00000710265.1:c.*198_*199delinsCT	ENSP00000518161.1:n.*198_*199delinsCT
ENST00000688158.2:n.1904_1905delinsCT
ENST00000688922.2:c.*999_*1000delinsCT	ENSP00000508742.2:n.*999_*1000delinsCT
ENST00000700021.1:c.1124_1125delinsCT	ENSP00000514757.1:p.Glu375Ala
ENST00000700022.1:c.*508_*509delinsCT	ENSP00000514758.1:n.*508_*509delinsCT
ENST00000700023.1:n.2327_2328delinsCT
ENST00000700024.1:n.2561_2562delinsCT
ENST00000706954.1:c.1169_1170delinsCT	ENSP00000516674.1:p.Glu390Ala
ENST00000706955.1:c.*1204_*1205delinsCT	ENSP00000516675.1:n.*1204_*1205delinsCT
ENST00000686459.1:c.*755_*756delinsCT	ENSP00000508909.1:n.*755_*756delinsCT
ENST00000688158.1:c.*1280_*1281delinsCT	ENSP00000509254.1:n.*1280_*1281delinsCT
ENST00000688308.1:c.1169_1170delinsCT	ENSP00000508752.1:p.Glu390Ala
ENST00000688922.1:c.1090_1091delinsCT
ENST00000693560.1:c.1688_1689delinsCT	ENSP00000509861.1:p.Glu563Ala
ENST00000371953.8:c.1169_1170delinsCT MANE Select	ENSP00000361021.3:p.Glu390Ala
ENST00000371953.7:c.1169_1170delinsCT	ENSP00000361021.3:p.Glu390Ala
NM_000314.5:c.1169_1170delinsCT	NP_000305.3:p.Glu390Ala
NM_000314.6:c.1169_1170delinsCT	NP_000305.3:p.Glu390Ala
NM_001304717.2:c.1688_1689delinsCT	NP_001291646.2:p.Glu563Ala
NM_001304718.1:c.578_579delinsCT	NP_001291647.1:p.Glu193Ala
XM_006717926.2:c.1124_1125delinsCT	XP_006717989.1:p.Glu375Ala
XM_011539982.1:c.1073_1074delinsCT	XP_011538284.1:p.Glu358Ala
XR_945791.1:n.1739_1740delinsCT
NM_000314.7:c.1169_1170delinsCT	NP_000305.3:p.Glu390Ala
NM_001304717.5:c.1688_1689delinsCT	NP_001291646.4:p.Glu563Ala
NM_001304718.2:c.578_579delinsCT	NP_001291647.1:p.Glu193Ala
NM_000314.8:c.1169_1170delinsCT MANE Select	NP_000305.3:p.Glu390Ala