Canonical Allele Identifier: CA891841566

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965323_87965325delinsTCA , CM000672.2:g.87965323_87965325delinsTCA	GRCh38
NC_000010.10:g.89725080_89725082delinsTCA , CM000672.1:g.89725080_89725082delinsTCA	GRCh37
NC_000010.9:g.89715060_89715062delinsTCA	NCBI36
NG_007466.2:g.106885_106887delinsTCA , LRG_311:g.106885_106887delinsTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1156_1158delinsTCA	ENSP00000514759.2:p.Ser386=
ENST00000710265.1:c.*92_*94delinsTCA	ENSP00000518161.1:n.*92_*94delinsTCA
ENST00000688158.2:n.1798_1800delinsTCA
ENST00000688922.2:c.*893_*895delinsTCA	ENSP00000508742.2:n.*893_*895delinsTCA
ENST00000700021.1:c.1018_1020delinsTCA	ENSP00000514757.1:p.Ser340=
ENST00000700022.1:c.*402_*404delinsTCA	ENSP00000514758.1:n.*402_*404delinsTCA
ENST00000700023.1:n.2221_2223delinsTCA
ENST00000700024.1:n.2455_2457delinsTCA
ENST00000706954.1:c.1063_1065delinsTCA	ENSP00000516674.1:p.Ser355=
ENST00000706955.1:c.*1098_*1100delinsTCA	ENSP00000516675.1:n.*1098_*1100delinsTCA
ENST00000686459.1:c.*649_*651delinsTCA	ENSP00000508909.1:n.*649_*651delinsTCA
ENST00000688158.1:c.*1174_*1176delinsTCA	ENSP00000509254.1:n.*1174_*1176delinsTCA
ENST00000688308.1:c.1063_1065delinsTCA	ENSP00000508752.1:p.Ser355=
ENST00000688922.1:c.984_986delinsTCA
ENST00000693560.1:c.1582_1584delinsTCA	ENSP00000509861.1:p.Ser528=
ENST00000371953.8:c.1063_1065delinsTCA MANE Select	ENSP00000361021.3:p.Ser355=
ENST00000371953.7:c.1063_1065delinsTCA	ENSP00000361021.3:p.Ser355=
NM_000314.5:c.1063_1065delinsTCA	NP_000305.3:p.Ser355=
NM_000314.6:c.1063_1065delinsTCA	NP_000305.3:p.Ser355=
NM_001304717.2:c.1582_1584delinsTCA	NP_001291646.2:p.Ser528=
NM_001304718.1:c.472_474delinsTCA	NP_001291647.1:p.Ser158=
XM_006717926.2:c.1018_1020delinsTCA	XP_006717989.1:p.Ser340=
XM_011539982.1:c.967_969delinsTCA	XP_011538284.1:p.Ser323=
XR_945791.1:n.1633_1635delinsTCA
NM_000314.7:c.1063_1065delinsTCA	NP_000305.3:p.Ser355=
NM_001304717.5:c.1582_1584delinsTCA	NP_001291646.4:p.Ser528=
NM_001304718.2:c.472_474delinsTCA	NP_001291647.1:p.Ser158=
NM_000314.8:c.1063_1065delinsTCA MANE Select	NP_000305.3:p.Ser355=