Canonical Allele Identifier: CA2031002658

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40309121A= , CM000674.2:g.40309121A=	GRCh38
NC_000012.11:g.40702923A= , CM000674.1:g.40702923A=	GRCh37
NC_000012.10:g.38989190A=	NCBI36
NG_011709.1:g.89111A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4205A= MANE Select	ENSP00000298910.7:p.Tyr1402=
ENST00000679360.1:c.*3114A=	ENSP00000505368.1:n.*3114A=
ENST00000680790.1:c.3950A=	ENSP00000505335.1:p.Tyr1317=
ENST00000298910.11:c.4205A=	ENSP00000298910.7:p.Tyr1402=
ENST00000430804.5:c.1501A=
ENST00000479187.5:n.886A=
NM_198578.3:c.4205A=	NP_940980.3:p.Tyr1402=
XM_005268629.2:c.4205A=	XP_005268686.1:p.Tyr1402=
XM_011537877.1:c.4205A=	XP_011536179.1:p.Tyr1402=
XM_011537878.1:c.4205A=	XP_011536180.1:p.Tyr1402=
XM_011537879.1:c.3002A=	XP_011536181.1:p.Tyr1001=
XM_011537880.1:c.4205A=	XP_011536182.1:p.Tyr1402=
XM_011537881.1:c.4205A=	XP_011536183.1:p.Tyr1402=
XM_005268629.4:c.4205A=	XP_005268686.1:p.Tyr1402=
XM_011537877.3:c.4205A=	XP_011536179.1:p.Tyr1402=
XM_011537881.3:c.4205A=	XP_011536183.1:p.Tyr1402=
XM_017018786.2:c.4205A=	XP_016874275.1:p.Tyr1402=
XM_017018787.1:c.1121A=	XP_016874276.1:p.Tyr374=
XM_017018788.2:c.467A=	XP_016874277.1:p.Tyr156=
XM_024448833.1:c.3002A=	XP_024304601.1:p.Tyr1001=
XR_001748574.2:n.4447A=
NM_198578.4:c.4205A= MANE Select	NP_940980.4:p.Tyr1402=