Canonical Allele Identifier: CA2031006159

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40310435G= , CM000674.2:g.40310435G=	GRCh38
NC_000012.11:g.40704237G= , CM000674.1:g.40704237G=	GRCh37
NC_000012.10:g.38990504G=	NCBI36
NG_011709.1:g.90425G=

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.4322G= MANE Select	NP_940980.4:p.Arg1441=
ENST00000298910.12:c.4322G= MANE Select	ENSP00000298910.7:p.Arg1441=
NM_198578.3:c.4322G=	NP_940980.3:p.Arg1441=
ENST00000298910.11:c.4322G=	ENSP00000298910.7:p.Arg1441=
ENST00000430804.5:c.1618G=
ENST00000479187.5:n.1003G=
ENST00000679360.1:c.*3231G=	ENSP00000505368.1:n.*3231G=
ENST00000680790.1:c.4067G=	ENSP00000505335.1:p.Arg1356=
ENST00000681696.1:c.5G=	ENSP00000505871.1:p.Arg2=
XM_005268629.2:c.4322G=	XP_005268686.1:p.Arg1441=
XM_005268629.4:c.4322G=	XP_005268686.1:p.Arg1441=
XM_011537877.1:c.4322G=	XP_011536179.1:p.Arg1441=
XM_011537877.3:c.4322G=	XP_011536179.1:p.Arg1441=
XM_011537878.1:c.4322G=	XP_011536180.1:p.Arg1441=
XM_011537879.1:c.3119G=	XP_011536181.1:p.Arg1040=
XM_011537880.1:c.4322G=	XP_011536182.1:p.Arg1441=
XM_011537881.1:c.4322G=	XP_011536183.1:p.Arg1441=
XM_011537881.3:c.4322G=	XP_011536183.1:p.Arg1441=
XM_017018786.2:c.4322G=	XP_016874275.1:p.Arg1441=
XM_017018787.1:c.1238G=	XP_016874276.1:p.Arg413=
XM_017018788.2:c.584G=	XP_016874277.1:p.Arg195=
XM_024448833.1:c.3119G=	XP_024304601.1:p.Arg1040=
XR_001748574.2:n.4564G=