Canonical Allele Identifier: CA2031027345

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340448A= , CM000674.2:g.40340448A=	GRCh38
NC_000012.11:g.40734250A= , CM000674.1:g.40734250A=	GRCh37
NC_000012.10:g.39020517A=	NCBI36
NG_011709.1:g.120438A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6103A= MANE Select	ENSP00000298910.7:p.Thr2035=
ENST00000679360.1:c.*5012A=	ENSP00000505368.1:n.*5012A=
ENST00000679532.1:c.1877A=
ENST00000680018.1:c.1548A=	ENSP00000505347.1:n.1548A=
ENST00000680422.1:c.1748A=
ENST00000680425.1:c.1270A=	ENSP00000506459.1:n.1270A=
ENST00000680453.1:c.1560A=
ENST00000680790.1:c.5848A=	ENSP00000505335.1:p.Thr1950=
ENST00000681136.1:n.2087A=
ENST00000681696.1:c.1786A=	ENSP00000505871.1:p.Thr596=
ENST00000298910.11:c.6103A=	ENSP00000298910.7:p.Thr2035=
ENST00000430804.5:c.3399A=
ENST00000479187.5:n.2784A=
NM_198578.3:c.6103A=	NP_940980.3:p.Thr2035=
XM_005268629.2:c.6103A=	XP_005268686.1:p.Thr2035=
XM_011537877.1:c.6103A=	XP_011536179.1:p.Thr2035=
XM_011537878.1:c.6103A=	XP_011536180.1:p.Thr2035=
XM_011537879.1:c.4900A=	XP_011536181.1:p.Thr1634=
XM_005268629.4:c.6103A=	XP_005268686.1:p.Thr2035=
XM_011537877.3:c.6103A=	XP_011536179.1:p.Thr2035=
XM_017018787.1:c.3019A=	XP_016874276.1:p.Thr1007=
XM_017018788.2:c.2365A=	XP_016874277.1:p.Thr789=
XM_024448833.1:c.4900A=	XP_024304601.1:p.Thr1634=
NM_198578.4:c.6103A= MANE Select	NP_940980.4:p.Thr2035=