Canonical Allele Identifier: CA2030995014

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320097T= , CM000674.2:g.40320097T=	GRCh38
NC_000012.11:g.40713899T= , CM000674.1:g.40713899T=	GRCh37
NC_000012.10:g.39000166T=	NCBI36
NG_011709.1:g.100087T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4937T= MANE Select	ENSP00000298910.7:p.Met1646=
ENST00000679360.1:c.*3846T=	ENSP00000505368.1:n.*3846T=
ENST00000679532.1:c.711T=
ENST00000680018.1:c.382T=	ENSP00000505347.1:n.382T=
ENST00000680422.1:c.582T=
ENST00000680425.1:c.183-937T=	ENSP00000506459.1:n.183-937T=
ENST00000680453.1:c.473-937T=
ENST00000680790.1:c.4682T=	ENSP00000505335.1:p.Met1561=
ENST00000681136.1:n.921T=
ENST00000681696.1:c.620T=	ENSP00000505871.1:p.Met207=
ENST00000298910.11:c.4937T=	ENSP00000298910.7:p.Met1646=
ENST00000430804.5:c.2233T=
ENST00000479187.5:n.1618T=
NM_198578.3:c.4937T=	NP_940980.3:p.Met1646=
XM_005268629.2:c.4937T=	XP_005268686.1:p.Met1646=
XM_011537877.1:c.4937T=	XP_011536179.1:p.Met1646=
XM_011537878.1:c.4937T=	XP_011536180.1:p.Met1646=
XM_011537879.1:c.3734T=	XP_011536181.1:p.Met1245=
XM_011537881.1:c.4828-937T=	XP_011536183.1:n.4828-937T=
XM_005268629.4:c.4937T=	XP_005268686.1:p.Met1646=
XM_011537877.3:c.4937T=	XP_011536179.1:p.Met1646=
XM_011537881.3:c.4828-937T=	XP_011536183.1:n.4828-937T=
XM_017018787.1:c.1853T=	XP_016874276.1:p.Met618=
XM_017018788.2:c.1199T=	XP_016874277.1:p.Met400=
XM_024448833.1:c.3734T=	XP_024304601.1:p.Met1245=
XR_001748574.2:n.5305T=
NM_198578.4:c.4937T= MANE Select	NP_940980.4:p.Met1646=