Canonical Allele Identifier: CA2031000167

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351580G= , CM000674.2:g.40351580G=	GRCh38
NC_000012.11:g.40745382G= , CM000674.1:g.40745382G=	GRCh37
NC_000012.10:g.39031649G=	NCBI36
NG_011709.1:g.131570G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.6423G= MANE Select	ENSP00000298910.7:p.Thr2141=
ENST00000636518.1:c.220G=
ENST00000679360.1:c.*5332G=	ENSP00000505368.1:n.*5332G=
ENST00000679532.1:c.2197G=
ENST00000679683.1:c.213G=
ENST00000680018.1:c.1868G=	ENSP00000505347.1:n.1868G=
ENST00000680422.1:c.2068G=
ENST00000680425.1:c.1590G=	ENSP00000506459.1:n.1590G=
ENST00000680453.1:c.1880G=
ENST00000680790.1:c.6168G=	ENSP00000505335.1:p.Thr2056=
ENST00000681136.1:n.2407G=
ENST00000681696.1:c.2106G=	ENSP00000505871.1:p.Thr702=
ENST00000298910.11:c.6423G=	ENSP00000298910.7:p.Thr2141=
ENST00000430804.5:c.3719G=
ENST00000479187.5:n.3104G=
NM_198578.3:c.6423G=	NP_940980.3:p.Thr2141=
XM_005268629.2:c.6423G=	XP_005268686.1:p.Thr2141=
XM_011537877.1:c.6423G=	XP_011536179.1:p.Thr2141=
XM_011537878.1:c.6423G=	XP_011536180.1:p.Thr2141=
XM_011537879.1:c.5220G=	XP_011536181.1:p.Thr1740=
XM_005268629.4:c.6423G=	XP_005268686.1:p.Thr2141=
XM_011537877.3:c.6423G=	XP_011536179.1:p.Thr2141=
XM_017018787.1:c.3339G=	XP_016874276.1:p.Thr1113=
XM_017018788.2:c.2685G=	XP_016874277.1:p.Thr895=
XM_024448833.1:c.5220G=	XP_024304601.1:p.Thr1740=
NM_198578.4:c.6423G= MANE Select	NP_940980.4:p.Thr2141=