Canonical Allele Identifier: CA2030995162

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320150G= , CM000674.2:g.40320150G=	GRCh38
NC_000012.11:g.40713952G= , CM000674.1:g.40713952G=	GRCh37
NC_000012.10:g.39000219G=	NCBI36
NG_011709.1:g.100140G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4990G= MANE Select	ENSP00000298910.7:p.Glu1664=
ENST00000679360.1:c.*3899G=	ENSP00000505368.1:n.*3899G=
ENST00000679532.1:c.764G=
ENST00000680018.1:c.435G=	ENSP00000505347.1:n.435G=
ENST00000680422.1:c.635G=
ENST00000680425.1:c.183-884G=	ENSP00000506459.1:n.183-884G=
ENST00000680453.1:c.473-884G=
ENST00000680790.1:c.4735G=	ENSP00000505335.1:p.Glu1579=
ENST00000681136.1:n.974G=
ENST00000681696.1:c.673G=	ENSP00000505871.1:p.Glu225=
ENST00000298910.11:c.4990G=	ENSP00000298910.7:p.Glu1664=
ENST00000430804.5:c.2286G=
ENST00000479187.5:n.1671G=
NM_198578.3:c.4990G=	NP_940980.3:p.Glu1664=
XM_005268629.2:c.4990G=	XP_005268686.1:p.Glu1664=
XM_011537877.1:c.4990G=	XP_011536179.1:p.Glu1664=
XM_011537878.1:c.4990G=	XP_011536180.1:p.Glu1664=
XM_011537879.1:c.3787G=	XP_011536181.1:p.Glu1263=
XM_011537881.1:c.4828-884G=	XP_011536183.1:n.4828-884G=
XM_005268629.4:c.4990G=	XP_005268686.1:p.Glu1664=
XM_011537877.3:c.4990G=	XP_011536179.1:p.Glu1664=
XM_011537881.3:c.4828-884G=	XP_011536183.1:n.4828-884G=
XM_017018787.1:c.1906G=	XP_016874276.1:p.Glu636=
XM_017018788.2:c.1252G=	XP_016874277.1:p.Glu418=
XM_024448833.1:c.3787G=	XP_024304601.1:p.Glu1263=
XR_001748574.2:n.5358G=
NM_198578.4:c.4990G= MANE Select	NP_940980.4:p.Glu1664=