Canonical Allele Identifier: CA235343542
Gene: LRRK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753449
ClinVar RCV Id: RCV002361692
dbSNP Id: rs1014412473

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40351581A>G , CM000674.2:g.40351581A>G GRCh38
NC_000012.11:g.40745383A>G , CM000674.1:g.40745383A>G GRCh37
NC_000012.10:g.39031650A>G NCBI36
NG_011709.1:g.131571A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.6424A>G MANE Select ENSP00000298910.7:p.Arg2142Gly
ENST00000636518.1:c.221A>G
ENST00000679360.1:c.*5333A>G ENSP00000505368.1:n.*5333A>G
ENST00000679532.1:c.2198A>G
ENST00000679683.1:c.214A>G
ENST00000680018.1:c.1869A>G ENSP00000505347.1:n.1869A>G
ENST00000680422.1:c.2069A>G
ENST00000680425.1:c.1591A>G ENSP00000506459.1:n.1591A>G
ENST00000680453.1:c.1881A>G
ENST00000680790.1:c.6169A>G ENSP00000505335.1:p.Arg2057Gly
ENST00000681136.1:n.2408A>G
ENST00000681696.1:c.2107A>G ENSP00000505871.1:p.Arg703Gly
ENST00000298910.11:c.6424A>G ENSP00000298910.7:p.Arg2142Gly
ENST00000430804.5:c.3720A>G
ENST00000479187.5:n.3105A>G
NM_198578.3:c.6424A>G NP_940980.3:p.Arg2142Gly
XM_005268629.2:c.6424A>G XP_005268686.1:p.Arg2142Gly
XM_011537877.1:c.6424A>G XP_011536179.1:p.Arg2142Gly
XM_011537878.1:c.6424A>G XP_011536180.1:p.Arg2142Gly
XM_011537879.1:c.5221A>G XP_011536181.1:p.Arg1741Gly
XM_005268629.4:c.6424A>G XP_005268686.1:p.Arg2142Gly
XM_011537877.3:c.6424A>G XP_011536179.1:p.Arg2142Gly
XM_017018787.1:c.3340A>G XP_016874276.1:p.Arg1114Gly
XM_017018788.2:c.2686A>G XP_016874277.1:p.Arg896Gly
XM_024448833.1:c.5221A>G XP_024304601.1:p.Arg1741Gly
NM_198578.4:c.6424A>G MANE Select NP_940980.4:p.Arg2142Gly