Canonical Allele Identifier: CA2031027319

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340436A= , CM000674.2:g.40340436A=	GRCh38
NC_000012.11:g.40734238A= , CM000674.1:g.40734238A=	GRCh37
NC_000012.10:g.39020505A=	NCBI36
NG_011709.1:g.120426A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6091A= MANE Select	ENSP00000298910.7:p.Thr2031=
ENST00000679360.1:c.*5000A=	ENSP00000505368.1:n.*5000A=
ENST00000679532.1:c.1865A=
ENST00000680018.1:c.1536A=	ENSP00000505347.1:n.1536A=
ENST00000680422.1:c.1736A=
ENST00000680425.1:c.1258A=	ENSP00000506459.1:n.1258A=
ENST00000680453.1:c.1548A=
ENST00000680790.1:c.5836A=	ENSP00000505335.1:p.Thr1946=
ENST00000681136.1:n.2075A=
ENST00000681696.1:c.1774A=	ENSP00000505871.1:p.Thr592=
ENST00000298910.11:c.6091A=	ENSP00000298910.7:p.Thr2031=
ENST00000430804.5:c.3387A=
ENST00000479187.5:n.2772A=
NM_198578.3:c.6091A=	NP_940980.3:p.Thr2031=
XM_005268629.2:c.6091A=	XP_005268686.1:p.Thr2031=
XM_011537877.1:c.6091A=	XP_011536179.1:p.Thr2031=
XM_011537878.1:c.6091A=	XP_011536180.1:p.Thr2031=
XM_011537879.1:c.4888A=	XP_011536181.1:p.Thr1630=
XM_005268629.4:c.6091A=	XP_005268686.1:p.Thr2031=
XM_011537877.3:c.6091A=	XP_011536179.1:p.Thr2031=
XM_017018787.1:c.3007A=	XP_016874276.1:p.Thr1003=
XM_017018788.2:c.2353A=	XP_016874277.1:p.Thr785=
XM_024448833.1:c.4888A=	XP_024304601.1:p.Thr1630=
NM_198578.4:c.6091A= MANE Select	NP_940980.4:p.Thr2031=