Canonical Allele Identifier: CA384403496
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340302A>C , CM000674.2:g.40340302A>C GRCh38
NC_000012.11:g.40734104A>C , CM000674.1:g.40734104A>C GRCh37
NC_000012.10:g.39020371A>C NCBI36
NG_011709.1:g.120292A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5957A>C MANE Select ENSP00000298910.7:p.His1986Pro
ENST00000679360.1:c.*4866A>C ENSP00000505368.1:n.*4866A>C
ENST00000679532.1:c.1731A>C
ENST00000680018.1:c.1402A>C ENSP00000505347.1:n.1402A>C
ENST00000680422.1:c.1602A>C
ENST00000680425.1:c.1124A>C ENSP00000506459.1:n.1124A>C
ENST00000680453.1:c.1414A>C
ENST00000680790.1:c.5702A>C ENSP00000505335.1:p.His1901Pro
ENST00000681136.1:n.1941A>C
ENST00000681696.1:c.1640A>C ENSP00000505871.1:p.His547Pro
ENST00000298910.11:c.5957A>C ENSP00000298910.7:p.His1986Pro
ENST00000430804.5:c.3253A>C
ENST00000479187.5:n.2638A>C
NM_198578.3:c.5957A>C NP_940980.3:p.His1986Pro
XM_005268629.2:c.5957A>C XP_005268686.1:p.His1986Pro
XM_011537877.1:c.5957A>C XP_011536179.1:p.His1986Pro
XM_011537878.1:c.5957A>C XP_011536180.1:p.His1986Pro
XM_011537879.1:c.4754A>C XP_011536181.1:p.His1585Pro
XM_005268629.4:c.5957A>C XP_005268686.1:p.His1986Pro
XM_011537877.3:c.5957A>C XP_011536179.1:p.His1986Pro
XM_017018787.1:c.2873A>C XP_016874276.1:p.His958Pro
XM_017018788.2:c.2219A>C XP_016874277.1:p.His740Pro
XM_024448833.1:c.4754A>C XP_024304601.1:p.His1585Pro
NM_198578.4:c.5957A>C MANE Select NP_940980.4:p.His1986Pro