Canonical Allele Identifier: CA2030983059
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298794_40298795delinsTA , CM000674.2:g.40298794_40298795delinsTA GRCh38
NC_000012.11:g.40692596_40692597delinsTA , CM000674.1:g.40692596_40692597delinsTA GRCh37
NC_000012.10:g.38978863_38978864delinsTA NCBI36
NG_011709.1:g.78784_78785delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3347+301_3347+302delinsTA MANE Select ENSP00000298910.7:n.3347+301_3347+302delinsTA
ENST00000679360.1:c.*2256+301_*2256+302delinsTA ENSP00000505368.1:n.*2256+301_*2256+302delinsTA
ENST00000680790.1:c.3092+301_3092+302delinsTA ENSP00000505335.1:n.3092+301_3092+302delinsTA
ENST00000298910.11:c.3347+301_3347+302delinsTA ENSP00000298910.7:n.3347+301_3347+302delinsTA
ENST00000343742.6:c.3347+301_3347+302delinsTA ENSP00000341930.2:n.3347+301_3347+302delinsTA
ENST00000430804.5:c.391+301_391+302delinsTA
ENST00000479187.5:n.28+301_28+302delinsTA
NM_198578.3:c.3347+301_3347+302delinsTA NP_940980.3:n.3347+301_3347+302delinsTA
XM_005268629.2:c.3347+301_3347+302delinsTA XP_005268686.1:n.3347+301_3347+302delinsTA
XM_011537877.1:c.3347+301_3347+302delinsTA XP_011536179.1:n.3347+301_3347+302delinsTA
XM_011537878.1:c.3347+301_3347+302delinsTA XP_011536180.1:n.3347+301_3347+302delinsTA
XM_011537879.1:c.2144+301_2144+302delinsTA XP_011536181.1:n.2144+301_2144+302delinsTA
XM_011537880.1:c.3347+301_3347+302delinsTA XP_011536182.1:n.3347+301_3347+302delinsTA
XM_011537881.1:c.3347+301_3347+302delinsTA XP_011536183.1:n.3347+301_3347+302delinsTA
XM_011537882.1:c.3347+301_3347+302delinsTA XP_011536184.1:n.3347+301_3347+302delinsTA
XM_005268629.4:c.3347+301_3347+302delinsTA XP_005268686.1:n.3347+301_3347+302delinsTA
XM_011537877.3:c.3347+301_3347+302delinsTA XP_011536179.1:n.3347+301_3347+302delinsTA
XM_011537881.3:c.3347+301_3347+302delinsTA XP_011536183.1:n.3347+301_3347+302delinsTA
XM_011537882.3:c.3347+301_3347+302delinsTA XP_011536184.1:n.3347+301_3347+302delinsTA
XM_017018786.2:c.3347+301_3347+302delinsTA XP_016874275.1:n.3347+301_3347+302delinsTA
XM_017018787.1:c.263+301_263+302delinsTA XP_016874276.1:n.263+301_263+302delinsTA
XM_017018789.2:c.3347+301_3347+302delinsTA XP_016874278.1:n.3347+301_3347+302delinsTA
XM_024448833.1:c.2144+301_2144+302delinsTA XP_024304601.1:n.2144+301_2144+302delinsTA
XR_001748574.2:n.3589+301_3589+302delinsTA
NM_198578.4:c.3347+301_3347+302delinsTA MANE Select NP_940980.4:n.3347+301_3347+302delinsTA