Canonical Allele Identifier: CA1926174119

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965472A= , CM000672.2:g.87965472A=	GRCh38
NC_000010.10:g.89725229A= , CM000672.1:g.89725229A=	GRCh37
NC_000010.9:g.89715209A=	NCBI36
NG_007466.2:g.107034A= , LRG_311:g.107034A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1305A=	ENSP00000514759.2:p.Ter435=
ENST00000710265.1:c.*241A=	ENSP00000518161.1:n.*241A=
ENST00000688158.2:n.1947A=
ENST00000688922.2:c.*1042A=	ENSP00000508742.2:n.*1042A=
ENST00000700021.1:c.1167A=	ENSP00000514757.1:p.Ter389=
ENST00000700022.1:c.*551A=	ENSP00000514758.1:n.*551A=
ENST00000700023.1:n.2370A=
ENST00000700024.1:n.2604A=
ENST00000706954.1:c.1212A=	ENSP00000516674.1:p.Ter404=
ENST00000706955.1:c.*1247A=	ENSP00000516675.1:n.*1247A=
ENST00000686459.1:c.*798A=	ENSP00000508909.1:n.*798A=
ENST00000688158.1:c.*1323A=	ENSP00000509254.1:n.*1323A=
ENST00000688308.1:c.1212A=	ENSP00000508752.1:p.Ter404=
ENST00000688922.1:c.1133A=
ENST00000693560.1:c.1731A=	ENSP00000509861.1:p.Ter577=
ENST00000371953.8:c.1212A= MANE Select	ENSP00000361021.3:p.Ter404=
ENST00000371953.7:c.1212A=	ENSP00000361021.3:p.Ter404=
NM_000314.5:c.1212A=	NP_000305.3:p.Ter404=
NM_000314.6:c.1212A=	NP_000305.3:p.Ter404=
NM_001304717.2:c.1731A=	NP_001291646.2:p.Ter577=
NM_001304718.1:c.621A=	NP_001291647.1:p.Ter207=
XM_006717926.2:c.1167A=	XP_006717989.1:p.Ter389=
XM_011539982.1:c.1116A=	XP_011538284.1:p.Ter372=
XR_945791.1:n.1782A=
NM_000314.7:c.1212A=	NP_000305.3:p.Ter404=
NM_001304717.5:c.1731A=	NP_001291646.4:p.Ter577=
NM_001304718.2:c.621A=	NP_001291647.1:p.Ter207=
NM_000314.8:c.1212A= MANE Select	NP_000305.3:p.Ter404=