Canonical Allele Identifier: CA2031026015

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363526G= , CM000674.2:g.40363526G=	GRCh38
NC_000012.11:g.40757328G= , CM000674.1:g.40757328G=	GRCh37
NC_000012.10:g.39043595G=	NCBI36
NG_011709.1:g.143516G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7153G= MANE Select	ENSP00000298910.7:p.Gly2385=
ENST00000636518.1:c.950G=
ENST00000679360.1:c.*6062G=	ENSP00000505368.1:n.*6062G=
ENST00000679532.1:c.2927G=
ENST00000679683.1:c.943G=
ENST00000680018.1:c.2598G=	ENSP00000505347.1:n.2598G=
ENST00000680422.1:c.4240G=
ENST00000680425.1:c.2320G=	ENSP00000506459.1:n.2320G=
ENST00000680453.1:c.2610G=
ENST00000680790.1:c.6898G=	ENSP00000505335.1:p.Gly2300=
ENST00000681136.1:n.3137G=
ENST00000681696.1:c.2836G=	ENSP00000505871.1:p.Gly946=
ENST00000681773.1:n.360G=
ENST00000298910.11:c.7153G=	ENSP00000298910.7:p.Gly2385=
ENST00000430804.5:c.4449G=
ENST00000479187.5:n.3834G=
NM_198578.3:c.7153G=	NP_940980.3:p.Gly2385=
XM_005268629.2:c.7153G=	XP_005268686.1:p.Gly2385=
XM_011537877.1:c.7153G=	XP_011536179.1:p.Gly2385=
XM_011537879.1:c.5950G=	XP_011536181.1:p.Gly1984=
XR_944868.1:n.485-8699C=
XM_005268629.4:c.7153G=	XP_005268686.1:p.Gly2385=
XM_011537877.3:c.7153G=	XP_011536179.1:p.Gly2385=
XM_017018787.1:c.4069G=	XP_016874276.1:p.Gly1357=
XM_017018788.2:c.3415G=	XP_016874277.1:p.Gly1139=
XM_024448833.1:c.5950G=	XP_024304601.1:p.Gly1984=
XR_944868.2:n.485-8699C=
NM_198578.4:c.7153G= MANE Select	NP_940980.4:p.Gly2385=