Canonical Allele Identifier: CA1926174112

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965469C= , CM000672.2:g.87965469C=	GRCh38
NC_000010.10:g.89725226C= , CM000672.1:g.89725226C=	GRCh37
NC_000010.9:g.89715206C=	NCBI36
NG_007466.2:g.107031C= , LRG_311:g.107031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1302C=	ENSP00000514759.2:p.Val434=
ENST00000710265.1:c.*238C=	ENSP00000518161.1:n.*238C=
ENST00000688158.2:n.1944C=
ENST00000688922.2:c.*1039C=	ENSP00000508742.2:n.*1039C=
ENST00000700021.1:c.1164C=	ENSP00000514757.1:p.Val388=
ENST00000700022.1:c.*548C=	ENSP00000514758.1:n.*548C=
ENST00000700023.1:n.2367C=
ENST00000700024.1:n.2601C=
ENST00000706954.1:c.1209C=	ENSP00000516674.1:p.Val403=
ENST00000706955.1:c.*1244C=	ENSP00000516675.1:n.*1244C=
ENST00000686459.1:c.*795C=	ENSP00000508909.1:n.*795C=
ENST00000688158.1:c.*1320C=	ENSP00000509254.1:n.*1320C=
ENST00000688308.1:c.1209C=	ENSP00000508752.1:p.Val403=
ENST00000688922.1:c.1130C=
ENST00000693560.1:c.1728C=	ENSP00000509861.1:p.Val576=
ENST00000371953.8:c.1209C= MANE Select	ENSP00000361021.3:p.Val403=
ENST00000371953.7:c.1209C=	ENSP00000361021.3:p.Val403=
NM_000314.5:c.1209C=	NP_000305.3:p.Val403=
NM_000314.6:c.1209C=	NP_000305.3:p.Val403=
NM_001304717.2:c.1728C=	NP_001291646.2:p.Val576=
NM_001304718.1:c.618C=	NP_001291647.1:p.Val206=
XM_006717926.2:c.1164C=	XP_006717989.1:p.Val388=
XM_011539982.1:c.1113C=	XP_011538284.1:p.Val371=
XR_945791.1:n.1779C=
NM_000314.7:c.1209C=	NP_000305.3:p.Val403=
NM_001304717.5:c.1728C=	NP_001291646.4:p.Val576=
NM_001304718.2:c.618C=	NP_001291647.1:p.Val206=
NM_000314.8:c.1209C= MANE Select	NP_000305.3:p.Val403=