Canonical Allele Identifier: CA2030999894

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351495G= , CM000674.2:g.40351495G=	GRCh38
NC_000012.11:g.40745297G= , CM000674.1:g.40745297G=	GRCh37
NC_000012.10:g.39031564G=	NCBI36
NG_011709.1:g.131485G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6382-44G= MANE Select	ENSP00000298910.7:n.6382-44G=
ENST00000636518.1:c.179-44G=
ENST00000679360.1:c.*5291-44G=	ENSP00000505368.1:n.*5291-44G=
ENST00000679532.1:c.2156-44G=
ENST00000679683.1:c.172-44G=
ENST00000680018.1:c.1827-44G=	ENSP00000505347.1:n.1827-44G=
ENST00000680422.1:c.2027-44G=
ENST00000680425.1:c.1549-44G=	ENSP00000506459.1:n.1549-44G=
ENST00000680453.1:c.1839-44G=
ENST00000680790.1:c.6127-44G=	ENSP00000505335.1:n.6127-44G=
ENST00000681136.1:n.2366-44G=
ENST00000681696.1:c.2065-44G=	ENSP00000505871.1:n.2065-44G=
ENST00000298910.11:c.6382-44G=	ENSP00000298910.7:n.6382-44G=
ENST00000430804.5:c.3678-44G=
ENST00000479187.5:n.3063-44G=
NM_198578.3:c.6382-44G=	NP_940980.3:n.6382-44G=
XM_005268629.2:c.6382-44G=	XP_005268686.1:n.6382-44G=
XM_011537877.1:c.6382-44G=	XP_011536179.1:n.6382-44G=
XM_011537878.1:c.6382-44G=	XP_011536180.1:n.6382-44G=
XM_011537879.1:c.5179-44G=	XP_011536181.1:n.5179-44G=
XM_005268629.4:c.6382-44G=	XP_005268686.1:n.6382-44G=
XM_011537877.3:c.6382-44G=	XP_011536179.1:n.6382-44G=
XM_017018787.1:c.3298-44G=	XP_016874276.1:n.3298-44G=
XM_017018788.2:c.2644-44G=	XP_016874277.1:n.2644-44G=
XM_024448833.1:c.5179-44G=	XP_024304601.1:n.5179-44G=
NM_198578.4:c.6382-44G= MANE Select	NP_940980.4:n.6382-44G=