Canonical Allele Identifier: CA2031027233

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340373G= , CM000674.2:g.40340373G=	GRCh38
NC_000012.11:g.40734175G= , CM000674.1:g.40734175G=	GRCh37
NC_000012.10:g.39020442G=	NCBI36
NG_011709.1:g.120363G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6028G= MANE Select	ENSP00000298910.7:p.Ala2010=
ENST00000679360.1:c.*4937G=	ENSP00000505368.1:n.*4937G=
ENST00000679532.1:c.1802G=
ENST00000680018.1:c.1473G=	ENSP00000505347.1:n.1473G=
ENST00000680422.1:c.1673G=
ENST00000680425.1:c.1195G=	ENSP00000506459.1:n.1195G=
ENST00000680453.1:c.1485G=
ENST00000680790.1:c.5773G=	ENSP00000505335.1:p.Ala1925=
ENST00000681136.1:n.2012G=
ENST00000681696.1:c.1711G=	ENSP00000505871.1:p.Ala571=
ENST00000298910.11:c.6028G=	ENSP00000298910.7:p.Ala2010=
ENST00000430804.5:c.3324G=
ENST00000479187.5:n.2709G=
NM_198578.3:c.6028G=	NP_940980.3:p.Ala2010=
XM_005268629.2:c.6028G=	XP_005268686.1:p.Ala2010=
XM_011537877.1:c.6028G=	XP_011536179.1:p.Ala2010=
XM_011537878.1:c.6028G=	XP_011536180.1:p.Ala2010=
XM_011537879.1:c.4825G=	XP_011536181.1:p.Ala1609=
XM_005268629.4:c.6028G=	XP_005268686.1:p.Ala2010=
XM_011537877.3:c.6028G=	XP_011536179.1:p.Ala2010=
XM_017018787.1:c.2944G=	XP_016874276.1:p.Ala982=
XM_017018788.2:c.2290G=	XP_016874277.1:p.Ala764=
XM_024448833.1:c.4825G=	XP_024304601.1:p.Ala1609=
NM_198578.4:c.6028G= MANE Select	NP_940980.4:p.Ala2010=