Canonical Allele Identifier: CA2031002694

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40309132C= , CM000674.2:g.40309132C=	GRCh38
NC_000012.11:g.40702934C= , CM000674.1:g.40702934C=	GRCh37
NC_000012.10:g.38989201C=	NCBI36
NG_011709.1:g.89122C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4216C= MANE Select	ENSP00000298910.7:p.Pro1406=
ENST00000679360.1:c.*3125C=	ENSP00000505368.1:n.*3125C=
ENST00000680790.1:c.3961C=	ENSP00000505335.1:p.Pro1321=
ENST00000298910.11:c.4216C=	ENSP00000298910.7:p.Pro1406=
ENST00000430804.5:c.1512C=
ENST00000479187.5:n.897C=
NM_198578.3:c.4216C=	NP_940980.3:p.Pro1406=
XM_005268629.2:c.4216C=	XP_005268686.1:p.Pro1406=
XM_011537877.1:c.4216C=	XP_011536179.1:p.Pro1406=
XM_011537878.1:c.4216C=	XP_011536180.1:p.Pro1406=
XM_011537879.1:c.3013C=	XP_011536181.1:p.Pro1005=
XM_011537880.1:c.4216C=	XP_011536182.1:p.Pro1406=
XM_011537881.1:c.4216C=	XP_011536183.1:p.Pro1406=
XM_005268629.4:c.4216C=	XP_005268686.1:p.Pro1406=
XM_011537877.3:c.4216C=	XP_011536179.1:p.Pro1406=
XM_011537881.3:c.4216C=	XP_011536183.1:p.Pro1406=
XM_017018786.2:c.4216C=	XP_016874275.1:p.Pro1406=
XM_017018787.1:c.1132C=	XP_016874276.1:p.Pro378=
XM_017018788.2:c.478C=	XP_016874277.1:p.Pro160=
XM_024448833.1:c.3013C=	XP_024304601.1:p.Pro1005=
XR_001748574.2:n.4458C=
NM_198578.4:c.4216C= MANE Select	NP_940980.4:p.Pro1406=