Canonical Allele Identifier: CA2031025744

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363412G= , CM000674.2:g.40363412G=	GRCh38
NC_000012.11:g.40757214G= , CM000674.1:g.40757214G=	GRCh37
NC_000012.10:g.39043481G=	NCBI36
NG_011709.1:g.143402G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7039G= MANE Select	ENSP00000298910.7:p.Ala2347=
ENST00000636518.1:c.836G=
ENST00000679360.1:c.*5948G=	ENSP00000505368.1:n.*5948G=
ENST00000679532.1:c.2813G=
ENST00000679683.1:c.829G=
ENST00000680018.1:c.2484G=	ENSP00000505347.1:n.2484G=
ENST00000680422.1:c.4126G=
ENST00000680425.1:c.2206G=	ENSP00000506459.1:n.2206G=
ENST00000680453.1:c.2496G=
ENST00000680790.1:c.6784G=	ENSP00000505335.1:p.Ala2262=
ENST00000681136.1:n.3023G=
ENST00000681696.1:c.2722G=	ENSP00000505871.1:p.Ala908=
ENST00000681773.1:n.246G=
ENST00000298910.11:c.7039G=	ENSP00000298910.7:p.Ala2347=
ENST00000430804.5:c.4335G=
ENST00000479187.5:n.3720G=
NM_198578.3:c.7039G=	NP_940980.3:p.Ala2347=
XM_005268629.2:c.7039G=	XP_005268686.1:p.Ala2347=
XM_011537877.1:c.7039G=	XP_011536179.1:p.Ala2347=
XM_011537879.1:c.5836G=	XP_011536181.1:p.Ala1946=
XR_944868.1:n.485-8585C=
XM_005268629.4:c.7039G=	XP_005268686.1:p.Ala2347=
XM_011537877.3:c.7039G=	XP_011536179.1:p.Ala2347=
XM_017018787.1:c.3955G=	XP_016874276.1:p.Ala1319=
XM_017018788.2:c.3301G=	XP_016874277.1:p.Ala1101=
XM_024448833.1:c.5836G=	XP_024304601.1:p.Ala1946=
XR_944868.2:n.485-8585C=
NM_198578.4:c.7039G= MANE Select	NP_940980.4:p.Ala2347=