Canonical Allele Identifier: CA2031025998

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363516A= , CM000674.2:g.40363516A=	GRCh38
NC_000012.11:g.40757318A= , CM000674.1:g.40757318A=	GRCh37
NC_000012.10:g.39043585A=	NCBI36
NG_011709.1:g.143506A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7143A= MANE Select	ENSP00000298910.7:p.Glu2381=
ENST00000636518.1:c.940A=
ENST00000679360.1:c.*6052A=	ENSP00000505368.1:n.*6052A=
ENST00000679532.1:c.2917A=
ENST00000679683.1:c.933A=
ENST00000680018.1:c.2588A=	ENSP00000505347.1:n.2588A=
ENST00000680422.1:c.4230A=
ENST00000680425.1:c.2310A=	ENSP00000506459.1:n.2310A=
ENST00000680453.1:c.2600A=
ENST00000680790.1:c.6888A=	ENSP00000505335.1:p.Glu2296=
ENST00000681136.1:n.3127A=
ENST00000681696.1:c.2826A=	ENSP00000505871.1:p.Glu942=
ENST00000681773.1:n.350A=
ENST00000298910.11:c.7143A=	ENSP00000298910.7:p.Glu2381=
ENST00000430804.5:c.4439A=
ENST00000479187.5:n.3824A=
NM_198578.3:c.7143A=	NP_940980.3:p.Glu2381=
XM_005268629.2:c.7143A=	XP_005268686.1:p.Glu2381=
XM_011537877.1:c.7143A=	XP_011536179.1:p.Glu2381=
XM_011537879.1:c.5940A=	XP_011536181.1:p.Glu1980=
XR_944868.1:n.485-8689T=
XM_005268629.4:c.7143A=	XP_005268686.1:p.Glu2381=
XM_011537877.3:c.7143A=	XP_011536179.1:p.Glu2381=
XM_017018787.1:c.4059A=	XP_016874276.1:p.Glu1353=
XM_017018788.2:c.3405A=	XP_016874277.1:p.Glu1135=
XM_024448833.1:c.5940A=	XP_024304601.1:p.Glu1980=
XR_944868.2:n.485-8689T=
NM_198578.4:c.7143A= MANE Select	NP_940980.4:p.Glu2381=