Canonical Allele Identifier: CA2031027221

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340366C= , CM000674.2:g.40340366C=	GRCh38
NC_000012.11:g.40734168C= , CM000674.1:g.40734168C=	GRCh37
NC_000012.10:g.39020435C=	NCBI36
NG_011709.1:g.120356C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6021C= MANE Select	ENSP00000298910.7:p.Pro2007=
ENST00000679360.1:c.*4930C=	ENSP00000505368.1:n.*4930C=
ENST00000679532.1:c.1795C=
ENST00000680018.1:c.1466C=	ENSP00000505347.1:n.1466C=
ENST00000680422.1:c.1666C=
ENST00000680425.1:c.1188C=	ENSP00000506459.1:n.1188C=
ENST00000680453.1:c.1478C=
ENST00000680790.1:c.5766C=	ENSP00000505335.1:p.Pro1922=
ENST00000681136.1:n.2005C=
ENST00000681696.1:c.1704C=	ENSP00000505871.1:p.Pro568=
ENST00000298910.11:c.6021C=	ENSP00000298910.7:p.Pro2007=
ENST00000430804.5:c.3317C=
ENST00000479187.5:n.2702C=
NM_198578.3:c.6021C=	NP_940980.3:p.Pro2007=
XM_005268629.2:c.6021C=	XP_005268686.1:p.Pro2007=
XM_011537877.1:c.6021C=	XP_011536179.1:p.Pro2007=
XM_011537878.1:c.6021C=	XP_011536180.1:p.Pro2007=
XM_011537879.1:c.4818C=	XP_011536181.1:p.Pro1606=
XM_005268629.4:c.6021C=	XP_005268686.1:p.Pro2007=
XM_011537877.3:c.6021C=	XP_011536179.1:p.Pro2007=
XM_017018787.1:c.2937C=	XP_016874276.1:p.Pro979=
XM_017018788.2:c.2283C=	XP_016874277.1:p.Pro761=
XM_024448833.1:c.4818C=	XP_024304601.1:p.Pro1606=
NM_198578.4:c.6021C= MANE Select	NP_940980.4:p.Pro2007=