Canonical Allele Identifier: CA2030995070

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320116C= , CM000674.2:g.40320116C=	GRCh38
NC_000012.11:g.40713918C= , CM000674.1:g.40713918C=	GRCh37
NC_000012.10:g.39000185C=	NCBI36
NG_011709.1:g.100106C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4956C= MANE Select	ENSP00000298910.7:p.Leu1652=
ENST00000679360.1:c.*3865C=	ENSP00000505368.1:n.*3865C=
ENST00000679532.1:c.730C=
ENST00000680018.1:c.401C=	ENSP00000505347.1:n.401C=
ENST00000680422.1:c.601C=
ENST00000680425.1:c.183-918C=	ENSP00000506459.1:n.183-918C=
ENST00000680453.1:c.473-918C=
ENST00000680790.1:c.4701C=	ENSP00000505335.1:p.Leu1567=
ENST00000681136.1:n.940C=
ENST00000681696.1:c.639C=	ENSP00000505871.1:p.Leu213=
ENST00000298910.11:c.4956C=	ENSP00000298910.7:p.Leu1652=
ENST00000430804.5:c.2252C=
ENST00000479187.5:n.1637C=
NM_198578.3:c.4956C=	NP_940980.3:p.Leu1652=
XM_005268629.2:c.4956C=	XP_005268686.1:p.Leu1652=
XM_011537877.1:c.4956C=	XP_011536179.1:p.Leu1652=
XM_011537878.1:c.4956C=	XP_011536180.1:p.Leu1652=
XM_011537879.1:c.3753C=	XP_011536181.1:p.Leu1251=
XM_011537881.1:c.4828-918C=	XP_011536183.1:n.4828-918C=
XM_005268629.4:c.4956C=	XP_005268686.1:p.Leu1652=
XM_011537877.3:c.4956C=	XP_011536179.1:p.Leu1652=
XM_011537881.3:c.4828-918C=	XP_011536183.1:n.4828-918C=
XM_017018787.1:c.1872C=	XP_016874276.1:p.Leu624=
XM_017018788.2:c.1218C=	XP_016874277.1:p.Leu406=
XM_024448833.1:c.3753C=	XP_024304601.1:p.Leu1251=
XR_001748574.2:n.5324C=
NM_198578.4:c.4956C= MANE Select	NP_940980.4:p.Leu1652=