Canonical Allele Identifier: CA2031002211

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40308935G= , CM000674.2:g.40308935G=	GRCh38
NC_000012.11:g.40702737G= , CM000674.1:g.40702737G=	GRCh37
NC_000012.10:g.38989004G=	NCBI36
NG_011709.1:g.88925G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4190-171G= MANE Select	ENSP00000298910.7:n.4190-171G=
ENST00000679360.1:c.*3099-171G=	ENSP00000505368.1:n.*3099-171G=
ENST00000680790.1:c.3935-171G=	ENSP00000505335.1:n.3935-171G=
ENST00000298910.11:c.4190-171G=	ENSP00000298910.7:n.4190-171G=
ENST00000430804.5:c.1486-171G=
ENST00000479187.5:n.871-171G=
NM_198578.3:c.4190-171G=	NP_940980.3:n.4190-171G=
XM_005268629.2:c.4190-171G=	XP_005268686.1:n.4190-171G=
XM_011537877.1:c.4190-171G=	XP_011536179.1:n.4190-171G=
XM_011537878.1:c.4190-171G=	XP_011536180.1:n.4190-171G=
XM_011537879.1:c.2987-171G=	XP_011536181.1:n.2987-171G=
XM_011537880.1:c.4190-171G=	XP_011536182.1:n.4190-171G=
XM_011537881.1:c.4190-171G=	XP_011536183.1:n.4190-171G=
XM_005268629.4:c.4190-171G=	XP_005268686.1:n.4190-171G=
XM_011537877.3:c.4190-171G=	XP_011536179.1:n.4190-171G=
XM_011537881.3:c.4190-171G=	XP_011536183.1:n.4190-171G=
XM_017018786.2:c.4190-171G=	XP_016874275.1:n.4190-171G=
XM_017018787.1:c.1106-171G=	XP_016874276.1:n.1106-171G=
XM_017018788.2:c.452-171G=	XP_016874277.1:n.452-171G=
XM_024448833.1:c.2987-171G=	XP_024304601.1:n.2987-171G=
XR_001748574.2:n.4432-171G=
NM_198578.4:c.4190-171G= MANE Select	NP_940980.4:n.4190-171G=