Canonical Allele Identifier: CA384415182
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298469A>C , CM000674.2:g.40298469A>C GRCh38
NC_000012.11:g.40692271A>C , CM000674.1:g.40692271A>C GRCh37
NC_000012.10:g.38978538A>C NCBI36
NG_011709.1:g.78459A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3323A>C MANE Select ENSP00000298910.7:p.Lys1108Thr
ENST00000679360.1:c.*2232A>C ENSP00000505368.1:n.*2232A>C
ENST00000680790.1:c.3068A>C ENSP00000505335.1:p.Lys1023Thr
ENST00000298910.11:c.3323A>C ENSP00000298910.7:p.Lys1108Thr
ENST00000343742.6:c.3323A>C ENSP00000341930.2:p.Lys1108Thr
ENST00000430804.5:c.367A>C
ENST00000479187.5:n.4A>C
NM_198578.3:c.3323A>C NP_940980.3:p.Lys1108Thr
XM_005268629.2:c.3323A>C XP_005268686.1:p.Lys1108Thr
XM_011537877.1:c.3323A>C XP_011536179.1:p.Lys1108Thr
XM_011537878.1:c.3323A>C XP_011536180.1:p.Lys1108Thr
XM_011537879.1:c.2120A>C XP_011536181.1:p.Lys707Thr
XM_011537880.1:c.3323A>C XP_011536182.1:p.Lys1108Thr
XM_011537881.1:c.3323A>C XP_011536183.1:p.Lys1108Thr
XM_011537882.1:c.3323A>C XP_011536184.1:p.Lys1108Thr
XM_005268629.4:c.3323A>C XP_005268686.1:p.Lys1108Thr
XM_011537877.3:c.3323A>C XP_011536179.1:p.Lys1108Thr
XM_011537881.3:c.3323A>C XP_011536183.1:p.Lys1108Thr
XM_011537882.3:c.3323A>C XP_011536184.1:p.Lys1108Thr
XM_017018786.2:c.3323A>C XP_016874275.1:p.Lys1108Thr
XM_017018787.1:c.239A>C XP_016874276.1:p.Lys80Thr
XM_017018789.2:c.3323A>C XP_016874278.1:p.Lys1108Thr
XM_024448833.1:c.2120A>C XP_024304601.1:p.Lys707Thr
XR_001748574.2:n.3565A>C
NM_198578.4:c.3323A>C MANE Select NP_940980.4:p.Lys1108Thr