Canonical Allele Identifier: CA2031025751

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363413C= , CM000674.2:g.40363413C=	GRCh38
NC_000012.11:g.40757215C= , CM000674.1:g.40757215C=	GRCh37
NC_000012.10:g.39043482C=	NCBI36
NG_011709.1:g.143403C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7040C= MANE Select	ENSP00000298910.7:p.Ala2347=
ENST00000636518.1:c.837C=
ENST00000679360.1:c.*5949C=	ENSP00000505368.1:n.*5949C=
ENST00000679532.1:c.2814C=
ENST00000679683.1:c.830C=
ENST00000680018.1:c.2485C=	ENSP00000505347.1:n.2485C=
ENST00000680422.1:c.4127C=
ENST00000680425.1:c.2207C=	ENSP00000506459.1:n.2207C=
ENST00000680453.1:c.2497C=
ENST00000680790.1:c.6785C=	ENSP00000505335.1:p.Ala2262=
ENST00000681136.1:n.3024C=
ENST00000681696.1:c.2723C=	ENSP00000505871.1:p.Ala908=
ENST00000681773.1:n.247C=
ENST00000298910.11:c.7040C=	ENSP00000298910.7:p.Ala2347=
ENST00000430804.5:c.4336C=
ENST00000479187.5:n.3721C=
NM_198578.3:c.7040C=	NP_940980.3:p.Ala2347=
XM_005268629.2:c.7040C=	XP_005268686.1:p.Ala2347=
XM_011537877.1:c.7040C=	XP_011536179.1:p.Ala2347=
XM_011537879.1:c.5837C=	XP_011536181.1:p.Ala1946=
XR_944868.1:n.485-8586G=
XM_005268629.4:c.7040C=	XP_005268686.1:p.Ala2347=
XM_011537877.3:c.7040C=	XP_011536179.1:p.Ala2347=
XM_017018787.1:c.3956C=	XP_016874276.1:p.Ala1319=
XM_017018788.2:c.3302C=	XP_016874277.1:p.Ala1101=
XM_024448833.1:c.5837C=	XP_024304601.1:p.Ala1946=
XR_944868.2:n.485-8586G=
NM_198578.4:c.7040C= MANE Select	NP_940980.4:p.Ala2347=