Canonical Allele Identifier: CA2031027204

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340357A= , CM000674.2:g.40340357A=	GRCh38
NC_000012.11:g.40734159A= , CM000674.1:g.40734159A=	GRCh37
NC_000012.10:g.39020426A=	NCBI36
NG_011709.1:g.120347A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6012A= MANE Select	ENSP00000298910.7:p.Thr2004=
ENST00000679360.1:c.*4921A=	ENSP00000505368.1:n.*4921A=
ENST00000679532.1:c.1786A=
ENST00000680018.1:c.1457A=	ENSP00000505347.1:n.1457A=
ENST00000680422.1:c.1657A=
ENST00000680425.1:c.1179A=	ENSP00000506459.1:n.1179A=
ENST00000680453.1:c.1469A=
ENST00000680790.1:c.5757A=	ENSP00000505335.1:p.Thr1919=
ENST00000681136.1:n.1996A=
ENST00000681696.1:c.1695A=	ENSP00000505871.1:p.Thr565=
ENST00000298910.11:c.6012A=	ENSP00000298910.7:p.Thr2004=
ENST00000430804.5:c.3308A=
ENST00000479187.5:n.2693A=
NM_198578.3:c.6012A=	NP_940980.3:p.Thr2004=
XM_005268629.2:c.6012A=	XP_005268686.1:p.Thr2004=
XM_011537877.1:c.6012A=	XP_011536179.1:p.Thr2004=
XM_011537878.1:c.6012A=	XP_011536180.1:p.Thr2004=
XM_011537879.1:c.4809A=	XP_011536181.1:p.Thr1603=
XM_005268629.4:c.6012A=	XP_005268686.1:p.Thr2004=
XM_011537877.3:c.6012A=	XP_011536179.1:p.Thr2004=
XM_017018787.1:c.2928A=	XP_016874276.1:p.Thr976=
XM_017018788.2:c.2274A=	XP_016874277.1:p.Thr758=
XM_024448833.1:c.4809A=	XP_024304601.1:p.Thr1603=
NM_198578.4:c.6012A= MANE Select	NP_940980.4:p.Thr2004=