Canonical Allele Identifier: CA2030996999

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40321114A= , CM000674.2:g.40321114A=	GRCh38
NC_000012.11:g.40714916A= , CM000674.1:g.40714916A=	GRCh37
NC_000012.10:g.39001183A=	NCBI36
NG_011709.1:g.101104A=

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.5096A= MANE Select	NP_940980.4:p.Tyr1699=
ENST00000298910.12:c.5096A= MANE Select	ENSP00000298910.7:p.Tyr1699=
NM_198578.3:c.5096A=	NP_940980.3:p.Tyr1699=
ENST00000298910.11:c.5096A=	ENSP00000298910.7:p.Tyr1699=
ENST00000430804.5:c.2392A=
ENST00000479187.5:n.1777A=
ENST00000679360.1:c.*4005A=	ENSP00000505368.1:n.*4005A=
ENST00000679532.1:c.870A=
ENST00000680018.1:c.541A=	ENSP00000505347.1:n.541A=
ENST00000680422.1:c.741A=
ENST00000680425.1:c.263A=	ENSP00000506459.1:n.263A=
ENST00000680453.1:c.553A=
ENST00000680790.1:c.4841A=	ENSP00000505335.1:p.Tyr1614=
ENST00000681136.1:n.1080A=
ENST00000681696.1:c.779A=	ENSP00000505871.1:p.Tyr260=
XM_005268629.2:c.5096A=	XP_005268686.1:p.Tyr1699=
XM_005268629.4:c.5096A=	XP_005268686.1:p.Tyr1699=
XM_011537877.1:c.5096A=	XP_011536179.1:p.Tyr1699=
XM_011537877.3:c.5096A=	XP_011536179.1:p.Tyr1699=
XM_011537878.1:c.5096A=	XP_011536180.1:p.Tyr1699=
XM_011537879.1:c.3893A=	XP_011536181.1:p.Tyr1298=
XM_011537881.1:c.*72A=	XP_011536183.1:n.*72A=
XM_011537881.3:c.*72A=	XP_011536183.1:n.*72A=
XM_017018787.1:c.2012A=	XP_016874276.1:p.Tyr671=
XM_017018788.2:c.1358A=	XP_016874277.1:p.Tyr453=
XM_024448833.1:c.3893A=	XP_024304601.1:p.Tyr1298=
XR_001748574.2:n.5464A=