Canonical Allele Identifier: CA2031000206

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351584C= , CM000674.2:g.40351584C=	GRCh38
NC_000012.11:g.40745386C= , CM000674.1:g.40745386C=	GRCh37
NC_000012.10:g.39031653C=	NCBI36
NG_011709.1:g.131574C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6427C= MANE Select	ENSP00000298910.7:p.Arg2143=
ENST00000636518.1:c.224C=
ENST00000679360.1:c.*5336C=	ENSP00000505368.1:n.*5336C=
ENST00000679532.1:c.2201C=
ENST00000679683.1:c.217C=
ENST00000680018.1:c.1872C=	ENSP00000505347.1:n.1872C=
ENST00000680422.1:c.2072C=
ENST00000680425.1:c.1594C=	ENSP00000506459.1:n.1594C=
ENST00000680453.1:c.1884C=
ENST00000680790.1:c.6172C=	ENSP00000505335.1:p.Arg2058=
ENST00000681136.1:n.2411C=
ENST00000681696.1:c.2110C=	ENSP00000505871.1:p.Arg704=
ENST00000298910.11:c.6427C=	ENSP00000298910.7:p.Arg2143=
ENST00000430804.5:c.3723C=
ENST00000479187.5:n.3108C=
NM_198578.3:c.6427C=	NP_940980.3:p.Arg2143=
XM_005268629.2:c.6427C=	XP_005268686.1:p.Arg2143=
XM_011537877.1:c.6427C=	XP_011536179.1:p.Arg2143=
XM_011537878.1:c.6427C=	XP_011536180.1:p.Arg2143=
XM_011537879.1:c.5224C=	XP_011536181.1:p.Arg1742=
XM_005268629.4:c.6427C=	XP_005268686.1:p.Arg2143=
XM_011537877.3:c.6427C=	XP_011536179.1:p.Arg2143=
XM_017018787.1:c.3343C=	XP_016874276.1:p.Arg1115=
XM_017018788.2:c.2689C=	XP_016874277.1:p.Arg897=
XM_024448833.1:c.5224C=	XP_024304601.1:p.Arg1742=
NM_198578.4:c.6427C= MANE Select	NP_940980.4:p.Arg2143=