Canonical Allele Identifier: CA384404034
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340416G>A , CM000674.2:g.40340416G>A GRCh38
NC_000012.11:g.40734218G>A , CM000674.1:g.40734218G>A GRCh37
NC_000012.10:g.39020485G>A NCBI36
NG_011709.1:g.120406G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.6071G>A MANE Select ENSP00000298910.7:p.Cys2024Tyr
ENST00000679360.1:c.*4980G>A ENSP00000505368.1:n.*4980G>A
ENST00000679532.1:c.1845G>A
ENST00000680018.1:c.1516G>A ENSP00000505347.1:n.1516G>A
ENST00000680422.1:c.1716G>A
ENST00000680425.1:c.1238G>A ENSP00000506459.1:n.1238G>A
ENST00000680453.1:c.1528G>A
ENST00000680790.1:c.5816G>A ENSP00000505335.1:p.Cys1939Tyr
ENST00000681136.1:n.2055G>A
ENST00000681696.1:c.1754G>A ENSP00000505871.1:p.Cys585Tyr
ENST00000298910.11:c.6071G>A ENSP00000298910.7:p.Cys2024Tyr
ENST00000430804.5:c.3367G>A
ENST00000479187.5:n.2752G>A
NM_198578.3:c.6071G>A NP_940980.3:p.Cys2024Tyr
XM_005268629.2:c.6071G>A XP_005268686.1:p.Cys2024Tyr
XM_011537877.1:c.6071G>A XP_011536179.1:p.Cys2024Tyr
XM_011537878.1:c.6071G>A XP_011536180.1:p.Cys2024Tyr
XM_011537879.1:c.4868G>A XP_011536181.1:p.Cys1623Tyr
XM_005268629.4:c.6071G>A XP_005268686.1:p.Cys2024Tyr
XM_011537877.3:c.6071G>A XP_011536179.1:p.Cys2024Tyr
XM_017018787.1:c.2987G>A XP_016874276.1:p.Cys996Tyr
XM_017018788.2:c.2333G>A XP_016874277.1:p.Cys778Tyr
XM_024448833.1:c.4868G>A XP_024304601.1:p.Cys1623Tyr
NM_198578.4:c.6071G>A MANE Select NP_940980.4:p.Cys2024Tyr