Canonical Allele Identifier: CA1926173956

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965387A= , CM000672.2:g.87965387A=	GRCh38
NC_000010.10:g.89725144A= , CM000672.1:g.89725144A=	GRCh37
NC_000010.9:g.89715124A=	NCBI36
NG_007466.2:g.106949A= , LRG_311:g.106949A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1220A=	ENSP00000514759.2:p.His407=
ENST00000710265.1:c.*156A=	ENSP00000518161.1:n.*156A=
ENST00000688158.2:n.1862A=
ENST00000688922.2:c.*957A=	ENSP00000508742.2:n.*957A=
ENST00000700021.1:c.1082A=	ENSP00000514757.1:p.His361=
ENST00000700022.1:c.*466A=	ENSP00000514758.1:n.*466A=
ENST00000700023.1:n.2285A=
ENST00000700024.1:n.2519A=
ENST00000706954.1:c.1127A=	ENSP00000516674.1:p.His376=
ENST00000706955.1:c.*1162A=	ENSP00000516675.1:n.*1162A=
ENST00000686459.1:c.*713A=	ENSP00000508909.1:n.*713A=
ENST00000688158.1:c.*1238A=	ENSP00000509254.1:n.*1238A=
ENST00000688308.1:c.1127A=	ENSP00000508752.1:p.His376=
ENST00000688922.1:c.1048A=
ENST00000693560.1:c.1646A=	ENSP00000509861.1:p.His549=
ENST00000371953.8:c.1127A= MANE Select	ENSP00000361021.3:p.His376=
ENST00000371953.7:c.1127A=	ENSP00000361021.3:p.His376=
NM_000314.5:c.1127A=	NP_000305.3:p.His376=
NM_000314.6:c.1127A=	NP_000305.3:p.His376=
NM_001304717.2:c.1646A=	NP_001291646.2:p.His549=
NM_001304718.1:c.536A=	NP_001291647.1:p.His179=
XM_006717926.2:c.1082A=	XP_006717989.1:p.His361=
XM_011539982.1:c.1031A=	XP_011538284.1:p.His344=
XR_945791.1:n.1697A=
NM_000314.7:c.1127A=	NP_000305.3:p.His376=
NM_001304717.5:c.1646A=	NP_001291646.4:p.His549=
NM_001304718.2:c.536A=	NP_001291647.1:p.His179=
NM_000314.8:c.1127A= MANE Select	NP_000305.3:p.His376=