Canonical Allele Identifier: CA891841662

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965428_87965430delinsTAT , CM000672.2:g.87965428_87965430delinsTAT	GRCh38
NC_000010.10:g.89725185_89725187delinsTAT , CM000672.1:g.89725185_89725187delinsTAT	GRCh37
NC_000010.9:g.89715165_89715167delinsTAT	NCBI36
NG_007466.2:g.106990_106992delinsTAT , LRG_311:g.106990_106992delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1261_1263delinsTAT	ENSP00000514759.2:p.Glu421Tyr
ENST00000710265.1:c.*197_*199delinsTAT	ENSP00000518161.1:n.*197_*199delinsTAT
ENST00000688158.2:n.1903_1905delinsTAT
ENST00000688922.2:c.*998_*1000delinsTAT	ENSP00000508742.2:n.*998_*1000delinsTAT
ENST00000700021.1:c.1123_1125delinsTAT	ENSP00000514757.1:p.Glu375Tyr
ENST00000700022.1:c.*507_*509delinsTAT	ENSP00000514758.1:n.*507_*509delinsTAT
ENST00000700023.1:n.2326_2328delinsTAT
ENST00000700024.1:n.2560_2562delinsTAT
ENST00000706954.1:c.1168_1170delinsTAT	ENSP00000516674.1:p.Glu390Tyr
ENST00000706955.1:c.*1203_*1205delinsTAT	ENSP00000516675.1:n.*1203_*1205delinsTAT
ENST00000686459.1:c.*754_*756delinsTAT	ENSP00000508909.1:n.*754_*756delinsTAT
ENST00000688158.1:c.*1279_*1281delinsTAT	ENSP00000509254.1:n.*1279_*1281delinsTAT
ENST00000688308.1:c.1168_1170delinsTAT	ENSP00000508752.1:p.Glu390Tyr
ENST00000688922.1:c.1089_1091delinsTAT
ENST00000693560.1:c.1687_1689delinsTAT	ENSP00000509861.1:p.Glu563Tyr
ENST00000371953.8:c.1168_1170delinsTAT MANE Select	ENSP00000361021.3:p.Glu390Tyr
ENST00000371953.7:c.1168_1170delinsTAT	ENSP00000361021.3:p.Glu390Tyr
NM_000314.5:c.1168_1170delinsTAT	NP_000305.3:p.Glu390Tyr
NM_000314.6:c.1168_1170delinsTAT	NP_000305.3:p.Glu390Tyr
NM_001304717.2:c.1687_1689delinsTAT	NP_001291646.2:p.Glu563Tyr
NM_001304718.1:c.577_579delinsTAT	NP_001291647.1:p.Glu193Tyr
XM_006717926.2:c.1123_1125delinsTAT	XP_006717989.1:p.Glu375Tyr
XM_011539982.1:c.1072_1074delinsTAT	XP_011538284.1:p.Glu358Tyr
XR_945791.1:n.1738_1740delinsTAT
NM_000314.7:c.1168_1170delinsTAT	NP_000305.3:p.Glu390Tyr
NM_001304717.5:c.1687_1689delinsTAT	NP_001291646.4:p.Glu563Tyr
NM_001304718.2:c.577_579delinsTAT	NP_001291647.1:p.Glu193Tyr
NM_000314.8:c.1168_1170delinsTAT MANE Select	NP_000305.3:p.Glu390Tyr