Canonical Allele Identifier: CA343677
Gene: LRRK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1943
dbSNP Id: rs34778348

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363526G>A , CM000674.2:g.40363526G>A GRCh38
NC_000012.11:g.40757328G>A , CM000674.1:g.40757328G>A GRCh37
NC_000012.10:g.39043595G>A NCBI36
NG_011709.1:g.143516G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7153G>A MANE Select ENSP00000298910.7:p.Gly2385Arg
ENST00000636518.1:n.950G>A
ENST00000679360.1:c.*6062G>A ENSP00000505368.1:n.*6062G>A
ENST00000679532.1:n.2927G>A
ENST00000679683.1:n.943G>A
ENST00000680018.1:n.2598G>A ENSP00000505347.1:n.2598G>A
ENST00000680422.1:n.4240G>A
ENST00000680425.1:n.2320G>A ENSP00000506459.1:n.2320G>A
ENST00000680453.1:n.2610G>A
ENST00000680790.1:c.6898G>A ENSP00000505335.1:p.Gly2300Arg
ENST00000681136.1:n.3137G>A
ENST00000681696.1:n.2836G>A ENSP00000505871.1:p.Gly946Arg
ENST00000681773.1:n.360G>A
ENST00000298910.11:c.7153G>A ENSP00000298910.7:p.Gly2385Arg
ENST00000430804.5:n.4449G>A
ENST00000479187.5:n.3834G>A
NM_198578.3:c.7153G>A NP_940980.3:p.Gly2385Arg
XM_005268629.2:c.7153G>A XP_005268686.1:p.Gly2385Arg
XM_011537877.1:c.7153G>A XP_011536179.1:p.Gly2385Arg
XM_011537879.1:c.5950G>A XP_011536181.1:p.Gly1984Arg
XR_944868.1:n.485-8699C>T
XM_005268629.4:c.7153G>A XP_005268686.1:p.Gly2385Arg
XM_011537877.3:c.7153G>A XP_011536179.1:p.Gly2385Arg
XM_017018787.1:c.4069G>A XP_016874276.1:p.Gly1357Arg
XM_017018788.2:c.3415G>A XP_016874277.1:p.Gly1139Arg
XM_024448833.1:c.5950G>A XP_024304601.1:p.Gly1984Arg
XR_944868.2:n.485-8699C>T
NM_198578.4:c.7153G>A MANE Select NP_940980.4:p.Gly2385Arg