Canonical Allele Identifier: CA2546998511
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40308898_40308919del , CM000674.2:g.40308898_40308919del GRCh38
NC_000012.11:g.40702700_40702721del , CM000674.1:g.40702700_40702721del GRCh37
NC_000012.10:g.38988967_38988988del NCBI36
NG_011709.1:g.88888_88909del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.4189+202_4190-187del MANE Select ENSP00000298910.7:n.4189+202_4190-187del
ENST00000679360.1:c.*3098+202_*3099-187del ENSP00000505368.1:n.*3098+202_*3099-187del
ENST00000680790.1:c.3934+202_3935-187del ENSP00000505335.1:n.3934+202_3935-187del
ENST00000298910.11:c.4189+202_4190-187del ENSP00000298910.7:n.4189+202_4190-187del
ENST00000430804.5:c.1485+202_1486-187del
ENST00000479187.5:n.870+202_871-187del
NM_198578.3:c.4189+202_4190-187del NP_940980.3:n.4189+202_4190-187del
XM_005268629.2:c.4189+202_4190-187del XP_005268686.1:n.4189+202_4190-187del
XM_011537877.1:c.4189+202_4190-187del XP_011536179.1:n.4189+202_4190-187del
XM_011537878.1:c.4189+202_4190-187del XP_011536180.1:n.4189+202_4190-187del
XM_011537879.1:c.2986+202_2987-187del XP_011536181.1:n.2986+202_2987-187del
XM_011537880.1:c.4189+202_4190-187del XP_011536182.1:n.4189+202_4190-187del
XM_011537881.1:c.4189+202_4190-187del XP_011536183.1:n.4189+202_4190-187del
XM_005268629.4:c.4189+202_4190-187del XP_005268686.1:n.4189+202_4190-187del
XM_011537877.3:c.4189+202_4190-187del XP_011536179.1:n.4189+202_4190-187del
XM_011537881.3:c.4189+202_4190-187del XP_011536183.1:n.4189+202_4190-187del
XM_017018786.2:c.4189+202_4190-187del XP_016874275.1:n.4189+202_4190-187del
XM_017018787.1:c.1105+202_1106-187del XP_016874276.1:n.1105+202_1106-187del
XM_017018788.2:c.451+202_452-187del XP_016874277.1:n.451+202_452-187del
XM_024448833.1:c.2986+202_2987-187del XP_024304601.1:n.2986+202_2987-187del
XR_001748574.2:n.4431+202_4432-187del
NM_198578.4:c.4189+202_4190-187del MANE Select NP_940980.4:n.4189+202_4190-187del