Canonical Allele Identifier: CA384404030
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340415T>C , CM000674.2:g.40340415T>C GRCh38
NC_000012.11:g.40734217T>C , CM000674.1:g.40734217T>C GRCh37
NC_000012.10:g.39020484T>C NCBI36
NG_011709.1:g.120405T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.6070T>C MANE Select ENSP00000298910.7:p.Cys2024Arg
ENST00000679360.1:c.*4979T>C ENSP00000505368.1:n.*4979T>C
ENST00000679532.1:c.1844T>C
ENST00000680018.1:c.1515T>C ENSP00000505347.1:n.1515T>C
ENST00000680422.1:c.1715T>C
ENST00000680425.1:c.1237T>C ENSP00000506459.1:n.1237T>C
ENST00000680453.1:c.1527T>C
ENST00000680790.1:c.5815T>C ENSP00000505335.1:p.Cys1939Arg
ENST00000681136.1:n.2054T>C
ENST00000681696.1:c.1753T>C ENSP00000505871.1:p.Cys585Arg
ENST00000298910.11:c.6070T>C ENSP00000298910.7:p.Cys2024Arg
ENST00000430804.5:c.3366T>C
ENST00000479187.5:n.2751T>C
NM_198578.3:c.6070T>C NP_940980.3:p.Cys2024Arg
XM_005268629.2:c.6070T>C XP_005268686.1:p.Cys2024Arg
XM_011537877.1:c.6070T>C XP_011536179.1:p.Cys2024Arg
XM_011537878.1:c.6070T>C XP_011536180.1:p.Cys2024Arg
XM_011537879.1:c.4867T>C XP_011536181.1:p.Cys1623Arg
XM_005268629.4:c.6070T>C XP_005268686.1:p.Cys2024Arg
XM_011537877.3:c.6070T>C XP_011536179.1:p.Cys2024Arg
XM_017018787.1:c.2986T>C XP_016874276.1:p.Cys996Arg
XM_017018788.2:c.2332T>C XP_016874277.1:p.Cys778Arg
XM_024448833.1:c.4867T>C XP_024304601.1:p.Cys1623Arg
NM_198578.4:c.6070T>C MANE Select NP_940980.4:p.Cys2024Arg