Canonical Allele Identifier: CA384403530
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340310A>T , CM000674.2:g.40340310A>T GRCh38
NC_000012.11:g.40734112A>T , CM000674.1:g.40734112A>T GRCh37
NC_000012.10:g.39020379A>T NCBI36
NG_011709.1:g.120300A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5965A>T MANE Select ENSP00000298910.7:p.Met1989Leu
ENST00000679360.1:c.*4874A>T ENSP00000505368.1:n.*4874A>T
ENST00000679532.1:c.1739A>T
ENST00000680018.1:c.1410A>T ENSP00000505347.1:n.1410A>T
ENST00000680422.1:c.1610A>T
ENST00000680425.1:c.1132A>T ENSP00000506459.1:n.1132A>T
ENST00000680453.1:c.1422A>T
ENST00000680790.1:c.5710A>T ENSP00000505335.1:p.Met1904Leu
ENST00000681136.1:n.1949A>T
ENST00000681696.1:c.1648A>T ENSP00000505871.1:p.Met550Leu
ENST00000298910.11:c.5965A>T ENSP00000298910.7:p.Met1989Leu
ENST00000430804.5:c.3261A>T
ENST00000479187.5:n.2646A>T
NM_198578.3:c.5965A>T NP_940980.3:p.Met1989Leu
XM_005268629.2:c.5965A>T XP_005268686.1:p.Met1989Leu
XM_011537877.1:c.5965A>T XP_011536179.1:p.Met1989Leu
XM_011537878.1:c.5965A>T XP_011536180.1:p.Met1989Leu
XM_011537879.1:c.4762A>T XP_011536181.1:p.Met1588Leu
XM_005268629.4:c.5965A>T XP_005268686.1:p.Met1989Leu
XM_011537877.3:c.5965A>T XP_011536179.1:p.Met1989Leu
XM_017018787.1:c.2881A>T XP_016874276.1:p.Met961Leu
XM_017018788.2:c.2227A>T XP_016874277.1:p.Met743Leu
XM_024448833.1:c.4762A>T XP_024304601.1:p.Met1588Leu
NM_198578.4:c.5965A>T MANE Select NP_940980.4:p.Met1989Leu