Canonical Allele Identifier: CA384404040
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340417C>G , CM000674.2:g.40340417C>G GRCh38
NC_000012.11:g.40734219C>G , CM000674.1:g.40734219C>G GRCh37
NC_000012.10:g.39020486C>G NCBI36
NG_011709.1:g.120407C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.6072C>G MANE Select ENSP00000298910.7:p.Cys2024Trp
ENST00000679360.1:c.*4981C>G ENSP00000505368.1:n.*4981C>G
ENST00000679532.1:c.1846C>G
ENST00000680018.1:c.1517C>G ENSP00000505347.1:n.1517C>G
ENST00000680422.1:c.1717C>G
ENST00000680425.1:c.1239C>G ENSP00000506459.1:n.1239C>G
ENST00000680453.1:c.1529C>G
ENST00000680790.1:c.5817C>G ENSP00000505335.1:p.Cys1939Trp
ENST00000681136.1:n.2056C>G
ENST00000681696.1:c.1755C>G ENSP00000505871.1:p.Cys585Trp
ENST00000298910.11:c.6072C>G ENSP00000298910.7:p.Cys2024Trp
ENST00000430804.5:c.3368C>G
ENST00000479187.5:n.2753C>G
NM_198578.3:c.6072C>G NP_940980.3:p.Cys2024Trp
XM_005268629.2:c.6072C>G XP_005268686.1:p.Cys2024Trp
XM_011537877.1:c.6072C>G XP_011536179.1:p.Cys2024Trp
XM_011537878.1:c.6072C>G XP_011536180.1:p.Cys2024Trp
XM_011537879.1:c.4869C>G XP_011536181.1:p.Cys1623Trp
XM_005268629.4:c.6072C>G XP_005268686.1:p.Cys2024Trp
XM_011537877.3:c.6072C>G XP_011536179.1:p.Cys2024Trp
XM_017018787.1:c.2988C>G XP_016874276.1:p.Cys996Trp
XM_017018788.2:c.2334C>G XP_016874277.1:p.Cys778Trp
XM_024448833.1:c.4869C>G XP_024304601.1:p.Cys1623Trp
NM_198578.4:c.6072C>G MANE Select NP_940980.4:p.Cys2024Trp