Canonical Allele Identifier: CA2031025783

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363436A= , CM000674.2:g.40363436A=	GRCh38
NC_000012.11:g.40757238A= , CM000674.1:g.40757238A=	GRCh37
NC_000012.10:g.39043505A=	NCBI36
NG_011709.1:g.143426A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7063A= MANE Select	ENSP00000298910.7:p.Ile2355=
ENST00000636518.1:c.860A=
ENST00000679360.1:c.*5972A=	ENSP00000505368.1:n.*5972A=
ENST00000679532.1:c.2837A=
ENST00000679683.1:c.853A=
ENST00000680018.1:c.2508A=	ENSP00000505347.1:n.2508A=
ENST00000680422.1:c.4150A=
ENST00000680425.1:c.2230A=	ENSP00000506459.1:n.2230A=
ENST00000680453.1:c.2520A=
ENST00000680790.1:c.6808A=	ENSP00000505335.1:p.Ile2270=
ENST00000681136.1:n.3047A=
ENST00000681696.1:c.2746A=	ENSP00000505871.1:p.Ile916=
ENST00000681773.1:n.270A=
ENST00000298910.11:c.7063A=	ENSP00000298910.7:p.Ile2355=
ENST00000430804.5:c.4359A=
ENST00000479187.5:n.3744A=
NM_198578.3:c.7063A=	NP_940980.3:p.Ile2355=
XM_005268629.2:c.7063A=	XP_005268686.1:p.Ile2355=
XM_011537877.1:c.7063A=	XP_011536179.1:p.Ile2355=
XM_011537879.1:c.5860A=	XP_011536181.1:p.Ile1954=
XR_944868.1:n.485-8609T=
XM_005268629.4:c.7063A=	XP_005268686.1:p.Ile2355=
XM_011537877.3:c.7063A=	XP_011536179.1:p.Ile2355=
XM_017018787.1:c.3979A=	XP_016874276.1:p.Ile1327=
XM_017018788.2:c.3325A=	XP_016874277.1:p.Ile1109=
XM_024448833.1:c.5860A=	XP_024304601.1:p.Ile1954=
XR_944868.2:n.485-8609T=
NM_198578.4:c.7063A= MANE Select	NP_940980.4:p.Ile2355=