Canonical Allele Identifier: CA2031000587

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351687G= , CM000674.2:g.40351687G=	GRCh38
NC_000012.11:g.40745489G= , CM000674.1:g.40745489G=	GRCh37
NC_000012.10:g.39031756G=	NCBI36
NG_011709.1:g.131677G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6530G= MANE Select	ENSP00000298910.7:p.Gly2177=
ENST00000636518.1:c.327G=
ENST00000679360.1:c.*5439G=	ENSP00000505368.1:n.*5439G=
ENST00000679532.1:c.2304G=
ENST00000679683.1:c.320G=
ENST00000680018.1:c.1975G=	ENSP00000505347.1:n.1975G=
ENST00000680422.1:c.2175G=
ENST00000680425.1:c.1697G=	ENSP00000506459.1:n.1697G=
ENST00000680453.1:c.1987G=
ENST00000680790.1:c.6275G=	ENSP00000505335.1:p.Gly2092=
ENST00000681136.1:n.2514G=
ENST00000681696.1:c.2213G=	ENSP00000505871.1:p.Gly738=
ENST00000298910.11:c.6530G=	ENSP00000298910.7:p.Gly2177=
ENST00000430804.5:c.3826G=
ENST00000479187.5:n.3211G=
NM_198578.3:c.6530G=	NP_940980.3:p.Gly2177=
XM_005268629.2:c.6530G=	XP_005268686.1:p.Gly2177=
XM_011537877.1:c.6530G=	XP_011536179.1:p.Gly2177=
XM_011537878.1:c.6530G=	XP_011536180.1:p.Gly2177=
XM_011537879.1:c.5327G=	XP_011536181.1:p.Gly1776=
XM_005268629.4:c.6530G=	XP_005268686.1:p.Gly2177=
XM_011537877.3:c.6530G=	XP_011536179.1:p.Gly2177=
XM_017018787.1:c.3446G=	XP_016874276.1:p.Gly1149=
XM_017018788.2:c.2792G=	XP_016874277.1:p.Gly931=
XM_024448833.1:c.5327G=	XP_024304601.1:p.Gly1776=
NM_198578.4:c.6530G= MANE Select	NP_940980.4:p.Gly2177=