Canonical Allele Identifier: CA2031027297

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340416G= , CM000674.2:g.40340416G=	GRCh38
NC_000012.11:g.40734218G= , CM000674.1:g.40734218G=	GRCh37
NC_000012.10:g.39020485G=	NCBI36
NG_011709.1:g.120406G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6071G= MANE Select	ENSP00000298910.7:p.Cys2024=
ENST00000679360.1:c.*4980G=	ENSP00000505368.1:n.*4980G=
ENST00000679532.1:c.1845G=
ENST00000680018.1:c.1516G=	ENSP00000505347.1:n.1516G=
ENST00000680422.1:c.1716G=
ENST00000680425.1:c.1238G=	ENSP00000506459.1:n.1238G=
ENST00000680453.1:c.1528G=
ENST00000680790.1:c.5816G=	ENSP00000505335.1:p.Cys1939=
ENST00000681136.1:n.2055G=
ENST00000681696.1:c.1754G=	ENSP00000505871.1:p.Cys585=
ENST00000298910.11:c.6071G=	ENSP00000298910.7:p.Cys2024=
ENST00000430804.5:c.3367G=
ENST00000479187.5:n.2752G=
NM_198578.3:c.6071G=	NP_940980.3:p.Cys2024=
XM_005268629.2:c.6071G=	XP_005268686.1:p.Cys2024=
XM_011537877.1:c.6071G=	XP_011536179.1:p.Cys2024=
XM_011537878.1:c.6071G=	XP_011536180.1:p.Cys2024=
XM_011537879.1:c.4868G=	XP_011536181.1:p.Cys1623=
XM_005268629.4:c.6071G=	XP_005268686.1:p.Cys2024=
XM_011537877.3:c.6071G=	XP_011536179.1:p.Cys2024=
XM_017018787.1:c.2987G=	XP_016874276.1:p.Cys996=
XM_017018788.2:c.2333G=	XP_016874277.1:p.Cys778=
XM_024448833.1:c.4868G=	XP_024304601.1:p.Cys1623=
NM_198578.4:c.6071G= MANE Select	NP_940980.4:p.Cys2024=