Canonical Allele Identifier: CA1926189942

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960897A= , CM000672.2:g.87960897A=	GRCh38
NC_000010.10:g.89720654A= , CM000672.1:g.89720654A=	GRCh37
NC_000010.9:g.89710634A=	NCBI36
NG_007466.2:g.102459A= , LRG_311:g.102459A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.898A=	ENSP00000514759.2:p.Lys300=
ENST00000710265.1:c.805A=	ENSP00000518161.1:p.Lys269=
ENST00000472832.3:c.805A=	ENSP00000483066.2:p.Lys269=
ENST00000688158.2:n.1540A=
ENST00000688922.2:c.*635A=	ENSP00000508742.2:n.*635A=
ENST00000700021.1:c.760A=	ENSP00000514757.1:p.Lys254=
ENST00000700022.1:c.*144A=	ENSP00000514758.1:n.*144A=
ENST00000700023.1:n.1963A=
ENST00000700024.1:n.2197A=
ENST00000700025.1:n.1574A=
ENST00000700026.1:n.442A=
ENST00000700029.1:c.732A=
ENST00000706954.1:c.805A=	ENSP00000516674.1:p.Lys269=
ENST00000706955.1:c.*840A=	ENSP00000516675.1:n.*840A=
ENST00000686459.1:c.*391A=	ENSP00000508909.1:n.*391A=
ENST00000688158.1:c.*916A=	ENSP00000509254.1:n.*916A=
ENST00000688308.1:c.805A=	ENSP00000508752.1:p.Lys269=
ENST00000688922.1:c.726A=
ENST00000693560.1:c.1324A=	ENSP00000509861.1:p.Lys442=
ENST00000371953.8:c.805A= MANE Select	ENSP00000361021.3:p.Lys269=
ENST00000371953.7:c.805A=	ENSP00000361021.3:p.Lys269=
ENST00000472832.2:c.232A=	ENSP00000483066.1:p.Lys78=
NM_000314.5:c.805A=	NP_000305.3:p.Lys269=
NM_000314.6:c.805A=	NP_000305.3:p.Lys269=
NM_001304717.2:c.1324A=	NP_001291646.2:p.Lys442=
NM_001304718.1:c.214A=	NP_001291647.1:p.Lys72=
XM_006717926.2:c.760A=	XP_006717989.1:p.Lys254=
XM_011539981.1:c.805A=	XP_011538283.1:p.Lys269=
XM_011539982.1:c.709A=	XP_011538284.1:p.Lys237=
XR_945791.1:n.1375A=
NM_000314.7:c.805A=	NP_000305.3:p.Lys269=
NM_001304717.5:c.1324A=	NP_001291646.4:p.Lys442=
NM_001304718.2:c.214A=	NP_001291647.1:p.Lys72=
NM_000314.8:c.805A= MANE Select	NP_000305.3:p.Lys269=