Canonical Allele Identifier: CA2031025792

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363437T= , CM000674.2:g.40363437T=	GRCh38
NC_000012.11:g.40757239T= , CM000674.1:g.40757239T=	GRCh37
NC_000012.10:g.39043506T=	NCBI36
NG_011709.1:g.143427T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7064T= MANE Select	ENSP00000298910.7:p.Ile2355=
ENST00000636518.1:c.861T=
ENST00000679360.1:c.*5973T=	ENSP00000505368.1:n.*5973T=
ENST00000679532.1:c.2838T=
ENST00000679683.1:c.854T=
ENST00000680018.1:c.2509T=	ENSP00000505347.1:n.2509T=
ENST00000680422.1:c.4151T=
ENST00000680425.1:c.2231T=	ENSP00000506459.1:n.2231T=
ENST00000680453.1:c.2521T=
ENST00000680790.1:c.6809T=	ENSP00000505335.1:p.Ile2270=
ENST00000681136.1:n.3048T=
ENST00000681696.1:c.2747T=	ENSP00000505871.1:p.Ile916=
ENST00000681773.1:n.271T=
ENST00000298910.11:c.7064T=	ENSP00000298910.7:p.Ile2355=
ENST00000430804.5:c.4360T=
ENST00000479187.5:n.3745T=
NM_198578.3:c.7064T=	NP_940980.3:p.Ile2355=
XM_005268629.2:c.7064T=	XP_005268686.1:p.Ile2355=
XM_011537877.1:c.7064T=	XP_011536179.1:p.Ile2355=
XM_011537879.1:c.5861T=	XP_011536181.1:p.Ile1954=
XR_944868.1:n.485-8610A=
XM_005268629.4:c.7064T=	XP_005268686.1:p.Ile2355=
XM_011537877.3:c.7064T=	XP_011536179.1:p.Ile2355=
XM_017018787.1:c.3980T=	XP_016874276.1:p.Ile1327=
XM_017018788.2:c.3326T=	XP_016874277.1:p.Ile1109=
XM_024448833.1:c.5861T=	XP_024304601.1:p.Ile1954=
XR_944868.2:n.485-8610A=
NM_198578.4:c.7064T= MANE Select	NP_940980.4:p.Ile2355=