Canonical Allele Identifier: CA891838054

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965428_87965430delinsTCT , CM000672.2:g.87965428_87965430delinsTCT	GRCh38
NC_000010.10:g.89725185_89725187delinsTCT , CM000672.1:g.89725185_89725187delinsTCT	GRCh37
NC_000010.9:g.89715165_89715167delinsTCT	NCBI36
NG_007466.2:g.106990_106992delinsTCT , LRG_311:g.106990_106992delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1261_1263delinsTCT	ENSP00000514759.2:p.Glu421Ser
ENST00000710265.1:c.*197_*199delinsTCT	ENSP00000518161.1:n.*197_*199delinsTCT
ENST00000688158.2:n.1903_1905delinsTCT
ENST00000688922.2:c.*998_*1000delinsTCT	ENSP00000508742.2:n.*998_*1000delinsTCT
ENST00000700021.1:c.1123_1125delinsTCT	ENSP00000514757.1:p.Glu375Ser
ENST00000700022.1:c.*507_*509delinsTCT	ENSP00000514758.1:n.*507_*509delinsTCT
ENST00000700023.1:n.2326_2328delinsTCT
ENST00000700024.1:n.2560_2562delinsTCT
ENST00000706954.1:c.1168_1170delinsTCT	ENSP00000516674.1:p.Glu390Ser
ENST00000706955.1:c.*1203_*1205delinsTCT	ENSP00000516675.1:n.*1203_*1205delinsTCT
ENST00000686459.1:c.*754_*756delinsTCT	ENSP00000508909.1:n.*754_*756delinsTCT
ENST00000688158.1:c.*1279_*1281delinsTCT	ENSP00000509254.1:n.*1279_*1281delinsTCT
ENST00000688308.1:c.1168_1170delinsTCT	ENSP00000508752.1:p.Glu390Ser
ENST00000688922.1:c.1089_1091delinsTCT
ENST00000693560.1:c.1687_1689delinsTCT	ENSP00000509861.1:p.Glu563Ser
ENST00000371953.8:c.1168_1170delinsTCT MANE Select	ENSP00000361021.3:p.Glu390Ser
ENST00000371953.7:c.1168_1170delinsTCT	ENSP00000361021.3:p.Glu390Ser
NM_000314.5:c.1168_1170delinsTCT	NP_000305.3:p.Glu390Ser
NM_000314.6:c.1168_1170delinsTCT	NP_000305.3:p.Glu390Ser
NM_001304717.2:c.1687_1689delinsTCT	NP_001291646.2:p.Glu563Ser
NM_001304718.1:c.577_579delinsTCT	NP_001291647.1:p.Glu193Ser
XM_006717926.2:c.1123_1125delinsTCT	XP_006717989.1:p.Glu375Ser
XM_011539982.1:c.1072_1074delinsTCT	XP_011538284.1:p.Glu358Ser
XR_945791.1:n.1738_1740delinsTCT
NM_000314.7:c.1168_1170delinsTCT	NP_000305.3:p.Glu390Ser
NM_001304717.5:c.1687_1689delinsTCT	NP_001291646.4:p.Glu563Ser
NM_001304718.2:c.577_579delinsTCT	NP_001291647.1:p.Glu193Ser
NM_000314.8:c.1168_1170delinsTCT MANE Select	NP_000305.3:p.Glu390Ser