Canonical Allele Identifier: CA2031000190

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351583A= , CM000674.2:g.40351583A=	GRCh38
NC_000012.11:g.40745385A= , CM000674.1:g.40745385A=	GRCh37
NC_000012.10:g.39031652A=	NCBI36
NG_011709.1:g.131573A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6426A= MANE Select	ENSP00000298910.7:p.Arg2142=
ENST00000636518.1:c.223A=
ENST00000679360.1:c.*5335A=	ENSP00000505368.1:n.*5335A=
ENST00000679532.1:c.2200A=
ENST00000679683.1:c.216A=
ENST00000680018.1:c.1871A=	ENSP00000505347.1:n.1871A=
ENST00000680422.1:c.2071A=
ENST00000680425.1:c.1593A=	ENSP00000506459.1:n.1593A=
ENST00000680453.1:c.1883A=
ENST00000680790.1:c.6171A=	ENSP00000505335.1:p.Arg2057=
ENST00000681136.1:n.2410A=
ENST00000681696.1:c.2109A=	ENSP00000505871.1:p.Arg703=
ENST00000298910.11:c.6426A=	ENSP00000298910.7:p.Arg2142=
ENST00000430804.5:c.3722A=
ENST00000479187.5:n.3107A=
NM_198578.3:c.6426A=	NP_940980.3:p.Arg2142=
XM_005268629.2:c.6426A=	XP_005268686.1:p.Arg2142=
XM_011537877.1:c.6426A=	XP_011536179.1:p.Arg2142=
XM_011537878.1:c.6426A=	XP_011536180.1:p.Arg2142=
XM_011537879.1:c.5223A=	XP_011536181.1:p.Arg1741=
XM_005268629.4:c.6426A=	XP_005268686.1:p.Arg2142=
XM_011537877.3:c.6426A=	XP_011536179.1:p.Arg2142=
XM_017018787.1:c.3342A=	XP_016874276.1:p.Arg1114=
XM_017018788.2:c.2688A=	XP_016874277.1:p.Arg896=
XM_024448833.1:c.5223A=	XP_024304601.1:p.Arg1741=
NM_198578.4:c.6426A= MANE Select	NP_940980.4:p.Arg2142=