Canonical Allele Identifier: CA2030983110
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298809_40298820delinsTTATAATATATA , CM000674.2:g.40298809_40298820delinsTTATAATATATA GRCh38
NC_000012.11:g.40692611_40692622delinsTTATAATATATA , CM000674.1:g.40692611_40692622delinsTTATAATATATA GRCh37
NC_000012.10:g.38978878_38978889delinsTTATAATATATA NCBI36
NG_011709.1:g.78799_78810delinsTTATAATATATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3348-300_3348-289delinsTTATAATATATA MANE Select ENSP00000298910.7:n.3348-300_3348-289delinsTTATAATATATA
ENST00000679360.1:c.*2257-300_*2257-289delinsTTATAATATATA ENSP00000505368.1:n.*2257-300_*2257-289delinsTTATAATATATA
ENST00000680790.1:c.3093-300_3093-289delinsTTATAATATATA ENSP00000505335.1:n.3093-300_3093-289delinsTTATAATATATA
ENST00000298910.11:c.3348-300_3348-289delinsTTATAATATATA ENSP00000298910.7:n.3348-300_3348-289delinsTTATAATATATA
ENST00000343742.6:c.3348-300_3348-289delinsTTATAATATATA ENSP00000341930.2:n.3348-300_3348-289delinsTTATAATATATA
ENST00000430804.5:c.392-300_392-289delinsTTATAATATATA
ENST00000479187.5:n.29-300_29-289delinsTTATAATATATA
NM_198578.3:c.3348-300_3348-289delinsTTATAATATATA NP_940980.3:n.3348-300_3348-289delinsTTATAATATATA
XM_005268629.2:c.3348-300_3348-289delinsTTATAATATATA XP_005268686.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537877.1:c.3348-300_3348-289delinsTTATAATATATA XP_011536179.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537878.1:c.3348-300_3348-289delinsTTATAATATATA XP_011536180.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537879.1:c.2145-300_2145-289delinsTTATAATATATA XP_011536181.1:n.2145-300_2145-289delinsTTATAATATATA
XM_011537880.1:c.3348-300_3348-289delinsTTATAATATATA XP_011536182.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537881.1:c.3348-300_3348-289delinsTTATAATATATA XP_011536183.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537882.1:c.3348-300_3348-289delinsTTATAATATATA XP_011536184.1:n.3348-300_3348-289delinsTTATAATATATA
XM_005268629.4:c.3348-300_3348-289delinsTTATAATATATA XP_005268686.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537877.3:c.3348-300_3348-289delinsTTATAATATATA XP_011536179.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537881.3:c.3348-300_3348-289delinsTTATAATATATA XP_011536183.1:n.3348-300_3348-289delinsTTATAATATATA
XM_011537882.3:c.3348-300_3348-289delinsTTATAATATATA XP_011536184.1:n.3348-300_3348-289delinsTTATAATATATA
XM_017018786.2:c.3348-300_3348-289delinsTTATAATATATA XP_016874275.1:n.3348-300_3348-289delinsTTATAATATATA
XM_017018787.1:c.264-300_264-289delinsTTATAATATATA XP_016874276.1:n.264-300_264-289delinsTTATAATATATA
XM_017018789.2:c.3348-300_3348-289delinsTTATAATATATA XP_016874278.1:n.3348-300_3348-289delinsTTATAATATATA
XM_024448833.1:c.2145-300_2145-289delinsTTATAATATATA XP_024304601.1:n.2145-300_2145-289delinsTTATAATATATA
XR_001748574.2:n.3590-300_3590-289delinsTTATAATATATA
NM_198578.4:c.3348-300_3348-289delinsTTATAATATATA MANE Select NP_940980.4:n.3348-300_3348-289delinsTTATAATATATA