Canonical Allele Identifier: CA1926174181

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965495A= , CM000672.2:g.87965495A=	GRCh38
NC_000010.10:g.89725252A= , CM000672.1:g.89725252A=	GRCh37
NC_000010.9:g.89715232A=	NCBI36
NG_007466.2:g.107057A= , LRG_311:g.107057A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*23A=	ENSP00000514759.2:n.*23A=
ENST00000710265.1:c.*264A=	ENSP00000518161.1:n.*264A=
ENST00000688158.2:n.1970A=
ENST00000688922.2:c.*1065A=	ENSP00000508742.2:n.*1065A=
ENST00000700021.1:c.*23A=	ENSP00000514757.1:n.*23A=
ENST00000700022.1:c.*574A=	ENSP00000514758.1:n.*574A=
ENST00000700023.1:n.2393A=
ENST00000700024.1:n.2627A=
ENST00000706954.1:c.*23A=	ENSP00000516674.1:n.*23A=
ENST00000706955.1:c.*1270A=	ENSP00000516675.1:n.*1270A=
ENST00000686459.1:c.*821A=	ENSP00000508909.1:n.*821A=
ENST00000688158.1:c.*1346A=	ENSP00000509254.1:n.*1346A=
ENST00000688308.1:c.*23A=	ENSP00000508752.1:n.*23A=
ENST00000688922.1:c.1156A=
ENST00000693560.1:c.*23A=	ENSP00000509861.1:n.*23A=
ENST00000371953.8:c.*23A= MANE Select	ENSP00000361021.3:n.*23A=
ENST00000371953.7:c.*23A=	ENSP00000361021.3:n.*23A=
NM_000314.5:c.*23A=	NP_000305.3:n.*23A=
NM_000314.6:c.*23A=	NP_000305.3:n.*23A=
NM_001304717.2:c.*23A=	NP_001291646.2:n.*23A=
NM_001304718.1:c.*23A=	NP_001291647.1:n.*23A=
XM_006717926.2:c.*23A=	XP_006717989.1:n.*23A=
XM_011539982.1:c.*23A=	XP_011538284.1:n.*23A=
XR_945791.1:n.1805A=
NM_000314.7:c.*23A=	NP_000305.3:n.*23A=
NM_001304717.5:c.*23A=	NP_001291646.4:n.*23A=
NM_001304718.2:c.*23A=	NP_001291647.1:n.*23A=
NM_000314.8:c.*23A= MANE Select	NP_000305.3:n.*23A=