Canonical Allele Identifier: CA1926173638

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965326A= , CM000672.2:g.87965326A=	GRCh38
NC_000010.10:g.89725083A= , CM000672.1:g.89725083A=	GRCh37
NC_000010.9:g.89715063A=	NCBI36
NG_007466.2:g.106888A= , LRG_311:g.106888A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1159A=	ENSP00000514759.2:p.Asn387=
ENST00000710265.1:c.*95A=	ENSP00000518161.1:n.*95A=
ENST00000688158.2:n.1801A=
ENST00000688922.2:c.*896A=	ENSP00000508742.2:n.*896A=
ENST00000700021.1:c.1021A=	ENSP00000514757.1:p.Asn341=
ENST00000700022.1:c.*405A=	ENSP00000514758.1:n.*405A=
ENST00000700023.1:n.2224A=
ENST00000700024.1:n.2458A=
ENST00000706954.1:c.1066A=	ENSP00000516674.1:p.Asn356=
ENST00000706955.1:c.*1101A=	ENSP00000516675.1:n.*1101A=
ENST00000686459.1:c.*652A=	ENSP00000508909.1:n.*652A=
ENST00000688158.1:c.*1177A=	ENSP00000509254.1:n.*1177A=
ENST00000688308.1:c.1066A=	ENSP00000508752.1:p.Asn356=
ENST00000688922.1:c.987A=
ENST00000693560.1:c.1585A=	ENSP00000509861.1:p.Asn529=
ENST00000371953.8:c.1066A= MANE Select	ENSP00000361021.3:p.Asn356=
ENST00000371953.7:c.1066A=	ENSP00000361021.3:p.Asn356=
NM_000314.5:c.1066A=	NP_000305.3:p.Asn356=
NM_000314.6:c.1066A=	NP_000305.3:p.Asn356=
NM_001304717.2:c.1585A=	NP_001291646.2:p.Asn529=
NM_001304718.1:c.475A=	NP_001291647.1:p.Asn159=
XM_006717926.2:c.1021A=	XP_006717989.1:p.Asn341=
XM_011539982.1:c.970A=	XP_011538284.1:p.Asn324=
XR_945791.1:n.1636A=
NM_000314.7:c.1066A=	NP_000305.3:p.Asn356=
NM_001304717.5:c.1585A=	NP_001291646.4:p.Asn529=
NM_001304718.2:c.475A=	NP_001291647.1:p.Asn159=
NM_000314.8:c.1066A= MANE Select	NP_000305.3:p.Asn356=