Canonical Allele Identifier: CA1926174040

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965437G= , CM000672.2:g.87965437G=	GRCh38
NC_000010.10:g.89725194G= , CM000672.1:g.89725194G=	GRCh37
NC_000010.9:g.89715174G=	NCBI36
NG_007466.2:g.106999G= , LRG_311:g.106999G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1270G=	ENSP00000514759.2:p.Asp424=
ENST00000710265.1:c.*206G=	ENSP00000518161.1:n.*206G=
ENST00000688158.2:n.1912G=
ENST00000688922.2:c.*1007G=	ENSP00000508742.2:n.*1007G=
ENST00000700021.1:c.1132G=	ENSP00000514757.1:p.Asp378=
ENST00000700022.1:c.*516G=	ENSP00000514758.1:n.*516G=
ENST00000700023.1:n.2335G=
ENST00000700024.1:n.2569G=
ENST00000706954.1:c.1177G=	ENSP00000516674.1:p.Asp393=
ENST00000706955.1:c.*1212G=	ENSP00000516675.1:n.*1212G=
ENST00000686459.1:c.*763G=	ENSP00000508909.1:n.*763G=
ENST00000688158.1:c.*1288G=	ENSP00000509254.1:n.*1288G=
ENST00000688308.1:c.1177G=	ENSP00000508752.1:p.Asp393=
ENST00000688922.1:c.1098G=
ENST00000693560.1:c.1696G=	ENSP00000509861.1:p.Asp566=
ENST00000371953.8:c.1177G= MANE Select	ENSP00000361021.3:p.Asp393=
ENST00000371953.7:c.1177G=	ENSP00000361021.3:p.Asp393=
NM_000314.5:c.1177G=	NP_000305.3:p.Asp393=
NM_000314.6:c.1177G=	NP_000305.3:p.Asp393=
NM_001304717.2:c.1696G=	NP_001291646.2:p.Asp566=
NM_001304718.1:c.586G=	NP_001291647.1:p.Asp196=
XM_006717926.2:c.1132G=	XP_006717989.1:p.Asp378=
XM_011539982.1:c.1081G=	XP_011538284.1:p.Asp361=
XR_945791.1:n.1747G=
NM_000314.7:c.1177G=	NP_000305.3:p.Asp393=
NM_001304717.5:c.1696G=	NP_001291646.4:p.Asp566=
NM_001304718.2:c.586G=	NP_001291647.1:p.Asp196=
NM_000314.8:c.1177G= MANE Select	NP_000305.3:p.Asp393=