Canonical Allele Identifier: CA1630855595

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40367861T= , CM000674.2:g.40367861T=	GRCh38
NC_000012.11:g.40761663T= , CM000674.1:g.40761663T=	GRCh37
NC_000012.10:g.39047930T=	NCBI36
NG_011709.1:g.147851T=

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.*96T= MANE Select	NP_940980.4:n.*96T=
ENST00000298910.12:c.*96T= MANE Select	ENSP00000298910.7:n.*96T=
NM_198578.3:c.*96T=	NP_940980.3:n.*96T=
ENST00000298910.11:c.*96T=	ENSP00000298910.7:n.*96T=
ENST00000430804.5:c.4976T=
ENST00000479187.5:n.6882T=
ENST00000636518.1:c.1459T=
ENST00000679532.1:c.3454T=
ENST00000679683.1:c.1470T=
ENST00000680018.1:c.3125T=	ENSP00000505347.1:n.3125T=
ENST00000680422.1:c.7288T=
ENST00000680425.1:c.2775T=	ENSP00000506459.1:n.2775T=
ENST00000680453.1:c.3119T=
ENST00000680790.1:c.*96T=	ENSP00000505335.1:n.*96T=
ENST00000681136.1:n.3612T=
ENST00000681696.1:c.3359T=	ENSP00000505871.1:n.3359T=
ENST00000681773.1:n.3408T=
XM_005268629.2:c.*96T=	XP_005268686.1:n.*96T=
XM_005268629.4:c.*96T=	XP_005268686.1:n.*96T=
XM_011537877.1:c.*96T=	XP_011536179.1:n.*96T=
XM_011537877.3:c.*96T=	XP_011536179.1:n.*96T=
XM_011537879.1:c.*96T=	XP_011536181.1:n.*96T=
XM_017018787.1:c.*96T=	XP_016874276.1:n.*96T=
XM_017018788.2:c.*96T=	XP_016874277.1:n.*96T=
XM_024448833.1:c.*96T=	XP_024304601.1:n.*96T=
XR_944868.1:n.485-13034A=
XR_944868.2:n.485-13034A=