Canonical Allele Identifier: CA2031002120

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40308879G= , CM000674.2:g.40308879G=	GRCh38
NC_000012.11:g.40702681G= , CM000674.1:g.40702681G=	GRCh37
NC_000012.10:g.38988948G=	NCBI36
NG_011709.1:g.88869G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4189+183G= MANE Select	ENSP00000298910.7:n.4189+183G=
ENST00000679360.1:c.*3098+183G=	ENSP00000505368.1:n.*3098+183G=
ENST00000680790.1:c.3934+183G=	ENSP00000505335.1:n.3934+183G=
ENST00000298910.11:c.4189+183G=	ENSP00000298910.7:n.4189+183G=
ENST00000430804.5:c.1485+183G=
ENST00000479187.5:n.870+183G=
NM_198578.3:c.4189+183G=	NP_940980.3:n.4189+183G=
XM_005268629.2:c.4189+183G=	XP_005268686.1:n.4189+183G=
XM_011537877.1:c.4189+183G=	XP_011536179.1:n.4189+183G=
XM_011537878.1:c.4189+183G=	XP_011536180.1:n.4189+183G=
XM_011537879.1:c.2986+183G=	XP_011536181.1:n.2986+183G=
XM_011537880.1:c.4189+183G=	XP_011536182.1:n.4189+183G=
XM_011537881.1:c.4189+183G=	XP_011536183.1:n.4189+183G=
XM_005268629.4:c.4189+183G=	XP_005268686.1:n.4189+183G=
XM_011537877.3:c.4189+183G=	XP_011536179.1:n.4189+183G=
XM_011537881.3:c.4189+183G=	XP_011536183.1:n.4189+183G=
XM_017018786.2:c.4189+183G=	XP_016874275.1:n.4189+183G=
XM_017018787.1:c.1105+183G=	XP_016874276.1:n.1105+183G=
XM_017018788.2:c.451+183G=	XP_016874277.1:n.451+183G=
XM_024448833.1:c.2986+183G=	XP_024304601.1:n.2986+183G=
XR_001748574.2:n.4431+183G=
NM_198578.4:c.4189+183G= MANE Select	NP_940980.4:n.4189+183G=