Canonical Allele Identifier: CA1926174016

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965426A= , CM000672.2:g.87965426A=	GRCh38
NC_000010.10:g.89725183A= , CM000672.1:g.89725183A=	GRCh37
NC_000010.9:g.89715163A=	NCBI36
NG_007466.2:g.106988A= , LRG_311:g.106988A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1259A=	ENSP00000514759.2:p.Asn420=
ENST00000710265.1:c.*195A=	ENSP00000518161.1:n.*195A=
ENST00000688158.2:n.1901A=
ENST00000688922.2:c.*996A=	ENSP00000508742.2:n.*996A=
ENST00000700021.1:c.1121A=	ENSP00000514757.1:p.Asn374=
ENST00000700022.1:c.*505A=	ENSP00000514758.1:n.*505A=
ENST00000700023.1:n.2324A=
ENST00000700024.1:n.2558A=
ENST00000706954.1:c.1166A=	ENSP00000516674.1:p.Asn389=
ENST00000706955.1:c.*1201A=	ENSP00000516675.1:n.*1201A=
ENST00000686459.1:c.*752A=	ENSP00000508909.1:n.*752A=
ENST00000688158.1:c.*1277A=	ENSP00000509254.1:n.*1277A=
ENST00000688308.1:c.1166A=	ENSP00000508752.1:p.Asn389=
ENST00000688922.1:c.1087A=
ENST00000693560.1:c.1685A=	ENSP00000509861.1:p.Asn562=
ENST00000371953.8:c.1166A= MANE Select	ENSP00000361021.3:p.Asn389=
ENST00000371953.7:c.1166A=	ENSP00000361021.3:p.Asn389=
NM_000314.5:c.1166A=	NP_000305.3:p.Asn389=
NM_000314.6:c.1166A=	NP_000305.3:p.Asn389=
NM_001304717.2:c.1685A=	NP_001291646.2:p.Asn562=
NM_001304718.1:c.575A=	NP_001291647.1:p.Asn192=
XM_006717926.2:c.1121A=	XP_006717989.1:p.Asn374=
XM_011539982.1:c.1070A=	XP_011538284.1:p.Asn357=
XR_945791.1:n.1736A=
NM_000314.7:c.1166A=	NP_000305.3:p.Asn389=
NM_001304717.5:c.1685A=	NP_001291646.4:p.Asn562=
NM_001304718.2:c.575A=	NP_001291647.1:p.Asn192=
NM_000314.8:c.1166A= MANE Select	NP_000305.3:p.Asn389=