Canonical Allele Identifier: CA1926174163

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965485C= , CM000672.2:g.87965485C=	GRCh38
NC_000010.10:g.89725242C= , CM000672.1:g.89725242C=	GRCh37
NC_000010.9:g.89715222C=	NCBI36
NG_007466.2:g.107047C= , LRG_311:g.107047C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.*13C=	ENSP00000514759.2:n.*13C=
ENST00000710265.1:c.*254C=	ENSP00000518161.1:n.*254C=
ENST00000688158.2:n.1960C=
ENST00000688922.2:c.*1055C=	ENSP00000508742.2:n.*1055C=
ENST00000700021.1:c.*13C=	ENSP00000514757.1:n.*13C=
ENST00000700022.1:c.*564C=	ENSP00000514758.1:n.*564C=
ENST00000700023.1:n.2383C=
ENST00000700024.1:n.2617C=
ENST00000706954.1:c.*13C=	ENSP00000516674.1:n.*13C=
ENST00000706955.1:c.*1260C=	ENSP00000516675.1:n.*1260C=
ENST00000686459.1:c.*811C=	ENSP00000508909.1:n.*811C=
ENST00000688158.1:c.*1336C=	ENSP00000509254.1:n.*1336C=
ENST00000688308.1:c.*13C=	ENSP00000508752.1:n.*13C=
ENST00000688922.1:c.1146C=
ENST00000693560.1:c.*13C=	ENSP00000509861.1:n.*13C=
ENST00000371953.8:c.*13C= MANE Select	ENSP00000361021.3:n.*13C=
ENST00000371953.7:c.*13C=	ENSP00000361021.3:n.*13C=
NM_000314.5:c.*13C=	NP_000305.3:n.*13C=
NM_000314.6:c.*13C=	NP_000305.3:n.*13C=
NM_001304717.2:c.*13C=	NP_001291646.2:n.*13C=
NM_001304718.1:c.*13C=	NP_001291647.1:n.*13C=
XM_006717926.2:c.*13C=	XP_006717989.1:n.*13C=
XM_011539982.1:c.*13C=	XP_011538284.1:n.*13C=
XR_945791.1:n.1795C=
NM_000314.7:c.*13C=	NP_000305.3:n.*13C=
NM_001304717.5:c.*13C=	NP_001291646.4:n.*13C=
NM_001304718.2:c.*13C=	NP_001291647.1:n.*13C=
NM_000314.8:c.*13C= MANE Select	NP_000305.3:n.*13C=