Canonical Allele Identifier: CA2031027120

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340323G= , CM000674.2:g.40340323G=	GRCh38
NC_000012.11:g.40734125G= , CM000674.1:g.40734125G=	GRCh37
NC_000012.10:g.39020392G=	NCBI36
NG_011709.1:g.120313G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5978G= MANE Select	ENSP00000298910.7:p.Arg1993=
ENST00000679360.1:c.*4887G=	ENSP00000505368.1:n.*4887G=
ENST00000679532.1:c.1752G=
ENST00000680018.1:c.1423G=	ENSP00000505347.1:n.1423G=
ENST00000680422.1:c.1623G=
ENST00000680425.1:c.1145G=	ENSP00000506459.1:n.1145G=
ENST00000680453.1:c.1435G=
ENST00000680790.1:c.5723G=	ENSP00000505335.1:p.Arg1908=
ENST00000681136.1:n.1962G=
ENST00000681696.1:c.1661G=	ENSP00000505871.1:p.Arg554=
ENST00000298910.11:c.5978G=	ENSP00000298910.7:p.Arg1993=
ENST00000430804.5:c.3274G=
ENST00000479187.5:n.2659G=
NM_198578.3:c.5978G=	NP_940980.3:p.Arg1993=
XM_005268629.2:c.5978G=	XP_005268686.1:p.Arg1993=
XM_011537877.1:c.5978G=	XP_011536179.1:p.Arg1993=
XM_011537878.1:c.5978G=	XP_011536180.1:p.Arg1993=
XM_011537879.1:c.4775G=	XP_011536181.1:p.Arg1592=
XM_005268629.4:c.5978G=	XP_005268686.1:p.Arg1993=
XM_011537877.3:c.5978G=	XP_011536179.1:p.Arg1993=
XM_017018787.1:c.2894G=	XP_016874276.1:p.Arg965=
XM_017018788.2:c.2240G=	XP_016874277.1:p.Arg747=
XM_024448833.1:c.4775G=	XP_024304601.1:p.Arg1592=
NM_198578.4:c.5978G= MANE Select	NP_940980.4:p.Arg1993=