Canonical Allele Identifier: CA2030995143

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320144A= , CM000674.2:g.40320144A=	GRCh38
NC_000012.11:g.40713946A= , CM000674.1:g.40713946A=	GRCh37
NC_000012.10:g.39000213A=	NCBI36
NG_011709.1:g.100134A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4984A= MANE Select	ENSP00000298910.7:p.Ile1662=
ENST00000679360.1:c.*3893A=	ENSP00000505368.1:n.*3893A=
ENST00000679532.1:c.758A=
ENST00000680018.1:c.429A=	ENSP00000505347.1:n.429A=
ENST00000680422.1:c.629A=
ENST00000680425.1:c.183-890A=	ENSP00000506459.1:n.183-890A=
ENST00000680453.1:c.473-890A=
ENST00000680790.1:c.4729A=	ENSP00000505335.1:p.Ile1577=
ENST00000681136.1:n.968A=
ENST00000681696.1:c.667A=	ENSP00000505871.1:p.Ile223=
ENST00000298910.11:c.4984A=	ENSP00000298910.7:p.Ile1662=
ENST00000430804.5:c.2280A=
ENST00000479187.5:n.1665A=
NM_198578.3:c.4984A=	NP_940980.3:p.Ile1662=
XM_005268629.2:c.4984A=	XP_005268686.1:p.Ile1662=
XM_011537877.1:c.4984A=	XP_011536179.1:p.Ile1662=
XM_011537878.1:c.4984A=	XP_011536180.1:p.Ile1662=
XM_011537879.1:c.3781A=	XP_011536181.1:p.Ile1261=
XM_011537881.1:c.4828-890A=	XP_011536183.1:n.4828-890A=
XM_005268629.4:c.4984A=	XP_005268686.1:p.Ile1662=
XM_011537877.3:c.4984A=	XP_011536179.1:p.Ile1662=
XM_011537881.3:c.4828-890A=	XP_011536183.1:n.4828-890A=
XM_017018787.1:c.1900A=	XP_016874276.1:p.Ile634=
XM_017018788.2:c.1246A=	XP_016874277.1:p.Ile416=
XM_024448833.1:c.3781A=	XP_024304601.1:p.Ile1261=
XR_001748574.2:n.5352A=
NM_198578.4:c.4984A= MANE Select	NP_940980.4:p.Ile1662=