Canonical Allele Identifier: CA384413214
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363435C>G , CM000674.2:g.40363435C>G GRCh38
NC_000012.11:g.40757237C>G , CM000674.1:g.40757237C>G GRCh37
NC_000012.10:g.39043504C>G NCBI36
NG_011709.1:g.143425C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7062C>G MANE Select ENSP00000298910.7:p.Ile2354Met
ENST00000636518.1:c.859C>G
ENST00000679360.1:c.*5971C>G ENSP00000505368.1:n.*5971C>G
ENST00000679532.1:c.2836C>G
ENST00000679683.1:c.852C>G
ENST00000680018.1:c.2507C>G ENSP00000505347.1:n.2507C>G
ENST00000680422.1:c.4149C>G
ENST00000680425.1:c.2229C>G ENSP00000506459.1:n.2229C>G
ENST00000680453.1:c.2519C>G
ENST00000680790.1:c.6807C>G ENSP00000505335.1:p.Ile2269Met
ENST00000681136.1:n.3046C>G
ENST00000681696.1:c.2745C>G ENSP00000505871.1:p.Ile915Met
ENST00000681773.1:n.269C>G
ENST00000298910.11:c.7062C>G ENSP00000298910.7:p.Ile2354Met
ENST00000430804.5:c.4358C>G
ENST00000479187.5:n.3743C>G
NM_198578.3:c.7062C>G NP_940980.3:p.Ile2354Met
XM_005268629.2:c.7062C>G XP_005268686.1:p.Ile2354Met
XM_011537877.1:c.7062C>G XP_011536179.1:p.Ile2354Met
XM_011537879.1:c.5859C>G XP_011536181.1:p.Ile1953Met
XR_944868.1:n.485-8608G>C
XM_005268629.4:c.7062C>G XP_005268686.1:p.Ile2354Met
XM_011537877.3:c.7062C>G XP_011536179.1:p.Ile2354Met
XM_017018787.1:c.3978C>G XP_016874276.1:p.Ile1326Met
XM_017018788.2:c.3324C>G XP_016874277.1:p.Ile1108Met
XM_024448833.1:c.5859C>G XP_024304601.1:p.Ile1953Met
XR_944868.2:n.485-8608G>C
NM_198578.4:c.7062C>G MANE Select NP_940980.4:p.Ile2354Met