Canonical Allele Identifier: CA384403670

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734140A>G (hg19) ; chr12:g.40340338A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340338A>G , CM000674.2:g.40340338A>G	GRCh38
NC_000012.11:g.40734140A>G , CM000674.1:g.40734140A>G	GRCh37
NC_000012.10:g.39020407A>G	NCBI36
NG_011709.1:g.120328A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5993A>G MANE Select	ENSP00000298910.7:p.His1998Arg
ENST00000679360.1:c.*4902A>G	ENSP00000505368.1:n.*4902A>G
ENST00000679532.1:c.1767A>G
ENST00000680018.1:c.1438A>G	ENSP00000505347.1:n.1438A>G
ENST00000680422.1:c.1638A>G
ENST00000680425.1:c.1160A>G	ENSP00000506459.1:n.1160A>G
ENST00000680453.1:c.1450A>G
ENST00000680790.1:c.5738A>G	ENSP00000505335.1:p.His1913Arg
ENST00000681136.1:n.1977A>G
ENST00000681696.1:c.1676A>G	ENSP00000505871.1:p.His559Arg
ENST00000298910.11:c.5993A>G	ENSP00000298910.7:p.His1998Arg
ENST00000430804.5:c.3289A>G
ENST00000479187.5:n.2674A>G
NM_198578.3:c.5993A>G	NP_940980.3:p.His1998Arg
XM_005268629.2:c.5993A>G	XP_005268686.1:p.His1998Arg
XM_011537877.1:c.5993A>G	XP_011536179.1:p.His1998Arg
XM_011537878.1:c.5993A>G	XP_011536180.1:p.His1998Arg
XM_011537879.1:c.4790A>G	XP_011536181.1:p.His1597Arg
XM_005268629.4:c.5993A>G	XP_005268686.1:p.His1998Arg
XM_011537877.3:c.5993A>G	XP_011536179.1:p.His1998Arg
XM_017018787.1:c.2909A>G	XP_016874276.1:p.His970Arg
XM_017018788.2:c.2255A>G	XP_016874277.1:p.His752Arg
XM_024448833.1:c.4790A>G	XP_024304601.1:p.His1597Arg
NM_198578.4:c.5993A>G MANE Select	NP_940980.4:p.His1998Arg