Canonical Allele Identifier: CA1926189949

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960907A= , CM000672.2:g.87960907A=	GRCh38
NC_000010.10:g.89720664A= , CM000672.1:g.89720664A=	GRCh37
NC_000010.9:g.89710644A=	NCBI36
NG_007466.2:g.102469A= , LRG_311:g.102469A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.908A=	ENSP00000514759.2:p.His303=
ENST00000710265.1:c.815A=	ENSP00000518161.1:p.His272=
ENST00000472832.3:c.815A=	ENSP00000483066.2:p.His272=
ENST00000688158.2:n.1550A=
ENST00000688922.2:c.*645A=	ENSP00000508742.2:n.*645A=
ENST00000700021.1:c.770A=	ENSP00000514757.1:p.His257=
ENST00000700022.1:c.*154A=	ENSP00000514758.1:n.*154A=
ENST00000700023.1:n.1973A=
ENST00000700024.1:n.2207A=
ENST00000700025.1:n.1584A=
ENST00000700026.1:n.452A=
ENST00000700029.1:c.742A=
ENST00000706954.1:c.815A=	ENSP00000516674.1:p.His272=
ENST00000706955.1:c.*850A=	ENSP00000516675.1:n.*850A=
ENST00000686459.1:c.*401A=	ENSP00000508909.1:n.*401A=
ENST00000688158.1:c.*926A=	ENSP00000509254.1:n.*926A=
ENST00000688308.1:c.815A=	ENSP00000508752.1:p.His272=
ENST00000688922.1:c.736A=
ENST00000693560.1:c.1334A=	ENSP00000509861.1:p.His445=
ENST00000371953.8:c.815A= MANE Select	ENSP00000361021.3:p.His272=
ENST00000371953.7:c.815A=	ENSP00000361021.3:p.His272=
ENST00000472832.2:c.242A=	ENSP00000483066.1:p.His81=
NM_000314.5:c.815A=	NP_000305.3:p.His272=
NM_000314.6:c.815A=	NP_000305.3:p.His272=
NM_001304717.2:c.1334A=	NP_001291646.2:p.His445=
NM_001304718.1:c.224A=	NP_001291647.1:p.His75=
XM_006717926.2:c.770A=	XP_006717989.1:p.His257=
XM_011539981.1:c.815A=	XP_011538283.1:p.His272=
XM_011539982.1:c.719A=	XP_011538284.1:p.His240=
XR_945791.1:n.1385A=
NM_000314.7:c.815A=	NP_000305.3:p.His272=
NM_001304717.5:c.1334A=	NP_001291646.4:p.His445=
NM_001304718.2:c.224A=	NP_001291647.1:p.His75=
NM_000314.8:c.815A= MANE Select	NP_000305.3:p.His272=