Canonical Allele Identifier: CA384413206
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363434T>C , CM000674.2:g.40363434T>C GRCh38
NC_000012.11:g.40757236T>C , CM000674.1:g.40757236T>C GRCh37
NC_000012.10:g.39043503T>C NCBI36
NG_011709.1:g.143424T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7061T>C MANE Select ENSP00000298910.7:p.Ile2354Thr
ENST00000636518.1:c.858T>C
ENST00000679360.1:c.*5970T>C ENSP00000505368.1:n.*5970T>C
ENST00000679532.1:c.2835T>C
ENST00000679683.1:c.851T>C
ENST00000680018.1:c.2506T>C ENSP00000505347.1:n.2506T>C
ENST00000680422.1:c.4148T>C
ENST00000680425.1:c.2228T>C ENSP00000506459.1:n.2228T>C
ENST00000680453.1:c.2518T>C
ENST00000680790.1:c.6806T>C ENSP00000505335.1:p.Ile2269Thr
ENST00000681136.1:n.3045T>C
ENST00000681696.1:c.2744T>C ENSP00000505871.1:p.Ile915Thr
ENST00000681773.1:n.268T>C
ENST00000298910.11:c.7061T>C ENSP00000298910.7:p.Ile2354Thr
ENST00000430804.5:c.4357T>C
ENST00000479187.5:n.3742T>C
NM_198578.3:c.7061T>C NP_940980.3:p.Ile2354Thr
XM_005268629.2:c.7061T>C XP_005268686.1:p.Ile2354Thr
XM_011537877.1:c.7061T>C XP_011536179.1:p.Ile2354Thr
XM_011537879.1:c.5858T>C XP_011536181.1:p.Ile1953Thr
XR_944868.1:n.485-8607A>G
XM_005268629.4:c.7061T>C XP_005268686.1:p.Ile2354Thr
XM_011537877.3:c.7061T>C XP_011536179.1:p.Ile2354Thr
XM_017018787.1:c.3977T>C XP_016874276.1:p.Ile1326Thr
XM_017018788.2:c.3323T>C XP_016874277.1:p.Ile1108Thr
XM_024448833.1:c.5858T>C XP_024304601.1:p.Ile1953Thr
XR_944868.2:n.485-8607A>G
NM_198578.4:c.7061T>C MANE Select NP_940980.4:p.Ile2354Thr