Canonical Allele Identifier: CA1926173978

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965391T= , CM000672.2:g.87965391T=	GRCh38
NC_000010.10:g.89725148T= , CM000672.1:g.89725148T=	GRCh37
NC_000010.9:g.89715128T=	NCBI36
NG_007466.2:g.106953T= , LRG_311:g.106953T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1224T=	ENSP00000514759.2:p.Tyr408=
ENST00000710265.1:c.*160T=	ENSP00000518161.1:n.*160T=
ENST00000688158.2:n.1866T=
ENST00000688922.2:c.*961T=	ENSP00000508742.2:n.*961T=
ENST00000700021.1:c.1086T=	ENSP00000514757.1:p.Tyr362=
ENST00000700022.1:c.*470T=	ENSP00000514758.1:n.*470T=
ENST00000700023.1:n.2289T=
ENST00000700024.1:n.2523T=
ENST00000706954.1:c.1131T=	ENSP00000516674.1:p.Tyr377=
ENST00000706955.1:c.*1166T=	ENSP00000516675.1:n.*1166T=
ENST00000686459.1:c.*717T=	ENSP00000508909.1:n.*717T=
ENST00000688158.1:c.*1242T=	ENSP00000509254.1:n.*1242T=
ENST00000688308.1:c.1131T=	ENSP00000508752.1:p.Tyr377=
ENST00000688922.1:c.1052T=
ENST00000693560.1:c.1650T=	ENSP00000509861.1:p.Tyr550=
ENST00000371953.8:c.1131T= MANE Select	ENSP00000361021.3:p.Tyr377=
ENST00000371953.7:c.1131T=	ENSP00000361021.3:p.Tyr377=
NM_000314.5:c.1131T=	NP_000305.3:p.Tyr377=
NM_000314.6:c.1131T=	NP_000305.3:p.Tyr377=
NM_001304717.2:c.1650T=	NP_001291646.2:p.Tyr550=
NM_001304718.1:c.540T=	NP_001291647.1:p.Tyr180=
XM_006717926.2:c.1086T=	XP_006717989.1:p.Tyr362=
XM_011539982.1:c.1035T=	XP_011538284.1:p.Tyr345=
XR_945791.1:n.1701T=
NM_000314.7:c.1131T=	NP_000305.3:p.Tyr377=
NM_001304717.5:c.1650T=	NP_001291646.4:p.Tyr550=
NM_001304718.2:c.540T=	NP_001291647.1:p.Tyr180=
NM_000314.8:c.1131T= MANE Select	NP_000305.3:p.Tyr377=