Canonical Allele Identifier: CA946845014
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs1944508531

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298887_40298902del , CM000674.2:g.40298887_40298902del GRCh38
NC_000012.11:g.40692689_40692704del , CM000674.1:g.40692689_40692704del GRCh37
NC_000012.10:g.38978956_38978971del NCBI36
NG_011709.1:g.78877_78892del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3348-222_3348-207del MANE Select ENSP00000298910.7:n.3348-222_3348-207del
ENST00000679360.1:c.*2257-222_*2257-207del ENSP00000505368.1:n.*2257-222_*2257-207del
ENST00000680790.1:c.3093-222_3093-207del ENSP00000505335.1:n.3093-222_3093-207del
ENST00000298910.11:c.3348-222_3348-207del ENSP00000298910.7:n.3348-222_3348-207del
ENST00000343742.6:c.3348-222_3348-207del ENSP00000341930.2:n.3348-222_3348-207del
ENST00000430804.5:c.392-222_392-207del
ENST00000479187.5:n.29-222_29-207del
NM_198578.3:c.3348-222_3348-207del NP_940980.3:n.3348-222_3348-207del
XM_005268629.2:c.3348-222_3348-207del XP_005268686.1:n.3348-222_3348-207del
XM_011537877.1:c.3348-222_3348-207del XP_011536179.1:n.3348-222_3348-207del
XM_011537878.1:c.3348-222_3348-207del XP_011536180.1:n.3348-222_3348-207del
XM_011537879.1:c.2145-222_2145-207del XP_011536181.1:n.2145-222_2145-207del
XM_011537880.1:c.3348-222_3348-207del XP_011536182.1:n.3348-222_3348-207del
XM_011537881.1:c.3348-222_3348-207del XP_011536183.1:n.3348-222_3348-207del
XM_011537882.1:c.3348-222_3348-207del XP_011536184.1:n.3348-222_3348-207del
XM_005268629.4:c.3348-222_3348-207del XP_005268686.1:n.3348-222_3348-207del
XM_011537877.3:c.3348-222_3348-207del XP_011536179.1:n.3348-222_3348-207del
XM_011537881.3:c.3348-222_3348-207del XP_011536183.1:n.3348-222_3348-207del
XM_011537882.3:c.3348-222_3348-207del XP_011536184.1:n.3348-222_3348-207del
XM_017018786.2:c.3348-222_3348-207del XP_016874275.1:n.3348-222_3348-207del
XM_017018787.1:c.264-222_264-207del XP_016874276.1:n.264-222_264-207del
XM_017018789.2:c.3348-222_3348-207del XP_016874278.1:n.3348-222_3348-207del
XM_024448833.1:c.2145-222_2145-207del XP_024304601.1:n.2145-222_2145-207del
XR_001748574.2:n.3590-222_3590-207del
NM_198578.4:c.3348-222_3348-207del MANE Select NP_940980.4:n.3348-222_3348-207del