Canonical Allele Identifier: CA1926173974

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87965390A= , CM000672.2:g.87965390A=	GRCh38
NC_000010.10:g.89725147A= , CM000672.1:g.89725147A=	GRCh37
NC_000010.9:g.89715127A=	NCBI36
NG_007466.2:g.106952A= , LRG_311:g.106952A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1223A=	ENSP00000514759.2:p.Tyr408=
ENST00000710265.1:c.*159A=	ENSP00000518161.1:n.*159A=
ENST00000688158.2:n.1865A=
ENST00000688922.2:c.*960A=	ENSP00000508742.2:n.*960A=
ENST00000700021.1:c.1085A=	ENSP00000514757.1:p.Tyr362=
ENST00000700022.1:c.*469A=	ENSP00000514758.1:n.*469A=
ENST00000700023.1:n.2288A=
ENST00000700024.1:n.2522A=
ENST00000706954.1:c.1130A=	ENSP00000516674.1:p.Tyr377=
ENST00000706955.1:c.*1165A=	ENSP00000516675.1:n.*1165A=
ENST00000686459.1:c.*716A=	ENSP00000508909.1:n.*716A=
ENST00000688158.1:c.*1241A=	ENSP00000509254.1:n.*1241A=
ENST00000688308.1:c.1130A=	ENSP00000508752.1:p.Tyr377=
ENST00000688922.1:c.1051A=
ENST00000693560.1:c.1649A=	ENSP00000509861.1:p.Tyr550=
ENST00000371953.8:c.1130A= MANE Select	ENSP00000361021.3:p.Tyr377=
ENST00000371953.7:c.1130A=	ENSP00000361021.3:p.Tyr377=
NM_000314.5:c.1130A=	NP_000305.3:p.Tyr377=
NM_000314.6:c.1130A=	NP_000305.3:p.Tyr377=
NM_001304717.2:c.1649A=	NP_001291646.2:p.Tyr550=
NM_001304718.1:c.539A=	NP_001291647.1:p.Tyr180=
XM_006717926.2:c.1085A=	XP_006717989.1:p.Tyr362=
XM_011539982.1:c.1034A=	XP_011538284.1:p.Tyr345=
XR_945791.1:n.1700A=
NM_000314.7:c.1130A=	NP_000305.3:p.Tyr377=
NM_001304717.5:c.1649A=	NP_001291646.4:p.Tyr550=
NM_001304718.2:c.539A=	NP_001291647.1:p.Tyr180=
NM_000314.8:c.1130A= MANE Select	NP_000305.3:p.Tyr377=