Canonical Allele Identifier: CA2031025778

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363435C= , CM000674.2:g.40363435C=	GRCh38
NC_000012.11:g.40757237C= , CM000674.1:g.40757237C=	GRCh37
NC_000012.10:g.39043504C=	NCBI36
NG_011709.1:g.143425C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7062C= MANE Select	ENSP00000298910.7:p.Ile2354=
ENST00000636518.1:c.859C=
ENST00000679360.1:c.*5971C=	ENSP00000505368.1:n.*5971C=
ENST00000679532.1:c.2836C=
ENST00000679683.1:c.852C=
ENST00000680018.1:c.2507C=	ENSP00000505347.1:n.2507C=
ENST00000680422.1:c.4149C=
ENST00000680425.1:c.2229C=	ENSP00000506459.1:n.2229C=
ENST00000680453.1:c.2519C=
ENST00000680790.1:c.6807C=	ENSP00000505335.1:p.Ile2269=
ENST00000681136.1:n.3046C=
ENST00000681696.1:c.2745C=	ENSP00000505871.1:p.Ile915=
ENST00000681773.1:n.269C=
ENST00000298910.11:c.7062C=	ENSP00000298910.7:p.Ile2354=
ENST00000430804.5:c.4358C=
ENST00000479187.5:n.3743C=
NM_198578.3:c.7062C=	NP_940980.3:p.Ile2354=
XM_005268629.2:c.7062C=	XP_005268686.1:p.Ile2354=
XM_011537877.1:c.7062C=	XP_011536179.1:p.Ile2354=
XM_011537879.1:c.5859C=	XP_011536181.1:p.Ile1953=
XR_944868.1:n.485-8608G=
XM_005268629.4:c.7062C=	XP_005268686.1:p.Ile2354=
XM_011537877.3:c.7062C=	XP_011536179.1:p.Ile2354=
XM_017018787.1:c.3978C=	XP_016874276.1:p.Ile1326=
XM_017018788.2:c.3324C=	XP_016874277.1:p.Ile1108=
XM_024448833.1:c.5859C=	XP_024304601.1:p.Ile1953=
XR_944868.2:n.485-8608G=
NM_198578.4:c.7062C= MANE Select	NP_940980.4:p.Ile2354=