Canonical Allele Identifier: CA2030990510

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40346884A= , CM000674.2:g.40346884A=	GRCh38
NC_000012.11:g.40740686A= , CM000674.1:g.40740686A=	GRCh37
NC_000012.10:g.39026953A=	NCBI36
NG_011709.1:g.126874A=

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.6241A= MANE Select	NP_940980.4:p.Asn2081=
ENST00000298910.12:c.6241A= MANE Select	ENSP00000298910.7:p.Asn2081=
NM_198578.3:c.6241A=	NP_940980.3:p.Asn2081=
ENST00000298910.11:c.6241A=	ENSP00000298910.7:p.Asn2081=
ENST00000430804.5:c.3537A=
ENST00000479187.5:n.2922A=
ENST00000636518.1:c.38A=
ENST00000679360.1:c.*5150A=	ENSP00000505368.1:n.*5150A=
ENST00000679532.1:c.2015A=
ENST00000679683.1:c.132A=
ENST00000680018.1:c.1686A=	ENSP00000505347.1:n.1686A=
ENST00000680422.1:c.1886A=
ENST00000680425.1:c.1408A=	ENSP00000506459.1:n.1408A=
ENST00000680453.1:c.1698A=
ENST00000680790.1:c.5986A=	ENSP00000505335.1:p.Asn1996=
ENST00000681136.1:n.2225A=
ENST00000681696.1:c.1924A=	ENSP00000505871.1:p.Asn642=
XM_005268629.2:c.6241A=	XP_005268686.1:p.Asn2081=
XM_005268629.4:c.6241A=	XP_005268686.1:p.Asn2081=
XM_011537877.1:c.6241A=	XP_011536179.1:p.Asn2081=
XM_011537877.3:c.6241A=	XP_011536179.1:p.Asn2081=
XM_011537878.1:c.6241A=	XP_011536180.1:p.Asn2081=
XM_011537879.1:c.5038A=	XP_011536181.1:p.Asn1680=
XM_017018787.1:c.3157A=	XP_016874276.1:p.Asn1053=
XM_017018788.2:c.2503A=	XP_016874277.1:p.Asn835=
XM_024448833.1:c.5038A=	XP_024304601.1:p.Asn1680=