Canonical Allele Identifier: CA891837185

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965323_87965325delinsGTT , CM000672.2:g.87965323_87965325delinsGTT	GRCh38
NC_000010.10:g.89725080_89725082delinsGTT , CM000672.1:g.89725080_89725082delinsGTT	GRCh37
NC_000010.9:g.89715060_89715062delinsGTT	NCBI36
NG_007466.2:g.106885_106887delinsGTT , LRG_311:g.106885_106887delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1156_1158delinsGTT	ENSP00000514759.2:p.Ser386Val
ENST00000710265.1:c.*92_*94delinsGTT	ENSP00000518161.1:n.*92_*94delinsGTT
ENST00000688158.2:n.1798_1800delinsGTT
ENST00000688922.2:c.*893_*895delinsGTT	ENSP00000508742.2:n.*893_*895delinsGTT
ENST00000700021.1:c.1018_1020delinsGTT	ENSP00000514757.1:p.Ser340Val
ENST00000700022.1:c.*402_*404delinsGTT	ENSP00000514758.1:n.*402_*404delinsGTT
ENST00000700023.1:n.2221_2223delinsGTT
ENST00000700024.1:n.2455_2457delinsGTT
ENST00000706954.1:c.1063_1065delinsGTT	ENSP00000516674.1:p.Ser355Val
ENST00000706955.1:c.*1098_*1100delinsGTT	ENSP00000516675.1:n.*1098_*1100delinsGTT
ENST00000686459.1:c.*649_*651delinsGTT	ENSP00000508909.1:n.*649_*651delinsGTT
ENST00000688158.1:c.*1174_*1176delinsGTT	ENSP00000509254.1:n.*1174_*1176delinsGTT
ENST00000688308.1:c.1063_1065delinsGTT	ENSP00000508752.1:p.Ser355Val
ENST00000688922.1:c.984_986delinsGTT
ENST00000693560.1:c.1582_1584delinsGTT	ENSP00000509861.1:p.Ser528Val
ENST00000371953.8:c.1063_1065delinsGTT MANE Select	ENSP00000361021.3:p.Ser355Val
ENST00000371953.7:c.1063_1065delinsGTT	ENSP00000361021.3:p.Ser355Val
NM_000314.5:c.1063_1065delinsGTT	NP_000305.3:p.Ser355Val
NM_000314.6:c.1063_1065delinsGTT	NP_000305.3:p.Ser355Val
NM_001304717.2:c.1582_1584delinsGTT	NP_001291646.2:p.Ser528Val
NM_001304718.1:c.472_474delinsGTT	NP_001291647.1:p.Ser158Val
XM_006717926.2:c.1018_1020delinsGTT	XP_006717989.1:p.Ser340Val
XM_011539982.1:c.967_969delinsGTT	XP_011538284.1:p.Ser323Val
XR_945791.1:n.1633_1635delinsGTT
NM_000314.7:c.1063_1065delinsGTT	NP_000305.3:p.Ser355Val
NM_001304717.5:c.1582_1584delinsGTT	NP_001291646.4:p.Ser528Val
NM_001304718.2:c.472_474delinsGTT	NP_001291647.1:p.Ser158Val
NM_000314.8:c.1063_1065delinsGTT MANE Select	NP_000305.3:p.Ser355Val