Canonical Allele Identifier: CA384403534
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340311T>A , CM000674.2:g.40340311T>A GRCh38
NC_000012.11:g.40734113T>A , CM000674.1:g.40734113T>A GRCh37
NC_000012.10:g.39020380T>A NCBI36
NG_011709.1:g.120301T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5966T>A MANE Select ENSP00000298910.7:p.Met1989Lys
ENST00000679360.1:c.*4875T>A ENSP00000505368.1:n.*4875T>A
ENST00000679532.1:c.1740T>A
ENST00000680018.1:c.1411T>A ENSP00000505347.1:n.1411T>A
ENST00000680422.1:c.1611T>A
ENST00000680425.1:c.1133T>A ENSP00000506459.1:n.1133T>A
ENST00000680453.1:c.1423T>A
ENST00000680790.1:c.5711T>A ENSP00000505335.1:p.Met1904Lys
ENST00000681136.1:n.1950T>A
ENST00000681696.1:c.1649T>A ENSP00000505871.1:p.Met550Lys
ENST00000298910.11:c.5966T>A ENSP00000298910.7:p.Met1989Lys
ENST00000430804.5:c.3262T>A
ENST00000479187.5:n.2647T>A
NM_198578.3:c.5966T>A NP_940980.3:p.Met1989Lys
XM_005268629.2:c.5966T>A XP_005268686.1:p.Met1989Lys
XM_011537877.1:c.5966T>A XP_011536179.1:p.Met1989Lys
XM_011537878.1:c.5966T>A XP_011536180.1:p.Met1989Lys
XM_011537879.1:c.4763T>A XP_011536181.1:p.Met1588Lys
XM_005268629.4:c.5966T>A XP_005268686.1:p.Met1989Lys
XM_011537877.3:c.5966T>A XP_011536179.1:p.Met1989Lys
XM_017018787.1:c.2882T>A XP_016874276.1:p.Met961Lys
XM_017018788.2:c.2228T>A XP_016874277.1:p.Met743Lys
XM_024448833.1:c.4763T>A XP_024304601.1:p.Met1588Lys
NM_198578.4:c.5966T>A MANE Select NP_940980.4:p.Met1989Lys