Canonical Allele Identifier: CA2618255099
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40253099dup , CM000674.2:g.40253099dup GRCh38
NC_000012.11:g.40646901dup , CM000674.1:g.40646901dup GRCh37
NC_000012.10:g.38933168dup NCBI36
NG_011709.1:g.33089dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.1288+83dup MANE Select ENSP00000298910.7:n.1288+83dup
ENST00000679360.1:c.*197+83dup ENSP00000505368.1:n.*197+83dup
ENST00000680790.1:c.1288+83dup ENSP00000505335.1:n.1288+83dup
ENST00000298910.11:c.1288+83dup ENSP00000298910.7:n.1288+83dup
ENST00000343742.6:c.1288+83dup ENSP00000341930.2:n.1288+83dup
ENST00000416796.5:c.662+83dup ENSP00000398726.1:n.662+83dup
NM_198578.3:c.1288+83dup NP_940980.3:n.1288+83dup
XM_005268629.2:c.1288+83dup XP_005268686.1:n.1288+83dup
XM_011537877.1:c.1288+83dup XP_011536179.1:n.1288+83dup
XM_011537878.1:c.1288+83dup XP_011536180.1:n.1288+83dup
XM_011537879.1:c.85+83dup XP_011536181.1:n.85+83dup
XM_011537880.1:c.1288+83dup XP_011536182.1:n.1288+83dup
XM_011537881.1:c.1288+83dup XP_011536183.1:n.1288+83dup
XM_011537882.1:c.1288+83dup XP_011536184.1:n.1288+83dup
XM_005268629.4:c.1288+83dup XP_005268686.1:n.1288+83dup
XM_011537877.3:c.1288+83dup XP_011536179.1:n.1288+83dup
XM_011537881.3:c.1288+83dup XP_011536183.1:n.1288+83dup
XM_011537882.3:c.1288+83dup XP_011536184.1:n.1288+83dup
XM_017018786.2:c.1288+83dup XP_016874275.1:n.1288+83dup
XM_017018789.2:c.1288+83dup XP_016874278.1:n.1288+83dup
XM_024448833.1:c.85+83dup XP_024304601.1:n.85+83dup
XR_001748574.2:n.1530+83dup
NM_198578.4:c.1288+83dup MANE Select NP_940980.4:n.1288+83dup