Canonical Allele Identifier: CA384404072
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340422G>A , CM000674.2:g.40340422G>A GRCh38
NC_000012.11:g.40734224G>A , CM000674.1:g.40734224G>A GRCh37
NC_000012.10:g.39020491G>A NCBI36
NG_011709.1:g.120412G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.6077G>A MANE Select ENSP00000298910.7:p.Arg2026Lys
ENST00000679360.1:c.*4986G>A ENSP00000505368.1:n.*4986G>A
ENST00000679532.1:c.1851G>A
ENST00000680018.1:c.1522G>A ENSP00000505347.1:n.1522G>A
ENST00000680422.1:c.1722G>A
ENST00000680425.1:c.1244G>A ENSP00000506459.1:n.1244G>A
ENST00000680453.1:c.1534G>A
ENST00000680790.1:c.5822G>A ENSP00000505335.1:p.Arg1941Lys
ENST00000681136.1:n.2061G>A
ENST00000681696.1:c.1760G>A ENSP00000505871.1:p.Arg587Lys
ENST00000298910.11:c.6077G>A ENSP00000298910.7:p.Arg2026Lys
ENST00000430804.5:c.3373G>A
ENST00000479187.5:n.2758G>A
NM_198578.3:c.6077G>A NP_940980.3:p.Arg2026Lys
XM_005268629.2:c.6077G>A XP_005268686.1:p.Arg2026Lys
XM_011537877.1:c.6077G>A XP_011536179.1:p.Arg2026Lys
XM_011537878.1:c.6077G>A XP_011536180.1:p.Arg2026Lys
XM_011537879.1:c.4874G>A XP_011536181.1:p.Arg1625Lys
XM_005268629.4:c.6077G>A XP_005268686.1:p.Arg2026Lys
XM_011537877.3:c.6077G>A XP_011536179.1:p.Arg2026Lys
XM_017018787.1:c.2993G>A XP_016874276.1:p.Arg998Lys
XM_017018788.2:c.2339G>A XP_016874277.1:p.Arg780Lys
XM_024448833.1:c.4874G>A XP_024304601.1:p.Arg1625Lys
NM_198578.4:c.6077G>A MANE Select NP_940980.4:p.Arg2026Lys