Canonical Allele Identifier: CA1926174066

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965449C= , CM000672.2:g.87965449C=	GRCh38
NC_000010.10:g.89725206C= , CM000672.1:g.89725206C=	GRCh37
NC_000010.9:g.89715186C=	NCBI36
NG_007466.2:g.107011C= , LRG_311:g.107011C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1282C=	ENSP00000514759.2:p.His428=
ENST00000710265.1:c.*218C=	ENSP00000518161.1:n.*218C=
ENST00000688158.2:n.1924C=
ENST00000688922.2:c.*1019C=	ENSP00000508742.2:n.*1019C=
ENST00000700021.1:c.1144C=	ENSP00000514757.1:p.His382=
ENST00000700022.1:c.*528C=	ENSP00000514758.1:n.*528C=
ENST00000700023.1:n.2347C=
ENST00000700024.1:n.2581C=
ENST00000706954.1:c.1189C=	ENSP00000516674.1:p.His397=
ENST00000706955.1:c.*1224C=	ENSP00000516675.1:n.*1224C=
ENST00000686459.1:c.*775C=	ENSP00000508909.1:n.*775C=
ENST00000688158.1:c.*1300C=	ENSP00000509254.1:n.*1300C=
ENST00000688308.1:c.1189C=	ENSP00000508752.1:p.His397=
ENST00000688922.1:c.1110C=
ENST00000693560.1:c.1708C=	ENSP00000509861.1:p.His570=
ENST00000371953.8:c.1189C= MANE Select	ENSP00000361021.3:p.His397=
ENST00000371953.7:c.1189C=	ENSP00000361021.3:p.His397=
NM_000314.5:c.1189C=	NP_000305.3:p.His397=
NM_000314.6:c.1189C=	NP_000305.3:p.His397=
NM_001304717.2:c.1708C=	NP_001291646.2:p.His570=
NM_001304718.1:c.598C=	NP_001291647.1:p.His200=
XM_006717926.2:c.1144C=	XP_006717989.1:p.His382=
XM_011539982.1:c.1093C=	XP_011538284.1:p.His365=
XR_945791.1:n.1759C=
NM_000314.7:c.1189C=	NP_000305.3:p.His397=
NM_001304717.5:c.1708C=	NP_001291646.4:p.His570=
NM_001304718.2:c.598C=	NP_001291647.1:p.His200=
NM_000314.8:c.1189C= MANE Select	NP_000305.3:p.His397=