Canonical Allele Identifier: CA2618280671
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40263913_40263920dup , CM000674.2:g.40263913_40263920dup GRCh38
NC_000012.11:g.40657715_40657722dup , CM000674.1:g.40657715_40657722dup GRCh37
NC_000012.10:g.38943982_38943989dup NCBI36
NG_011709.1:g.43903_43910dup

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.1656+12_1656+19dup MANE Select ENSP00000298910.7:n.1656+12_1656+19dup
ENST00000679360.1:c.*565+12_*565+19dup ENSP00000505368.1:n.*565+12_*565+19dup
ENST00000680790.1:c.1401+12_1401+19dup ENSP00000505335.1:n.1401+12_1401+19dup
ENST00000298910.11:c.1656+12_1656+19dup ENSP00000298910.7:n.1656+12_1656+19dup
ENST00000343742.6:c.1656+12_1656+19dup ENSP00000341930.2:n.1656+12_1656+19dup
ENST00000416796.5:c.900+12_900+19dup ENSP00000398726.1:n.900+12_900+19dup
NM_198578.3:c.1656+12_1656+19dup NP_940980.3:n.1656+12_1656+19dup
XM_005268629.2:c.1656+12_1656+19dup XP_005268686.1:n.1656+12_1656+19dup
XM_011537877.1:c.1656+12_1656+19dup XP_011536179.1:n.1656+12_1656+19dup
XM_011537878.1:c.1656+12_1656+19dup XP_011536180.1:n.1656+12_1656+19dup
XM_011537879.1:c.453+12_453+19dup XP_011536181.1:n.453+12_453+19dup
XM_011537880.1:c.1656+12_1656+19dup XP_011536182.1:n.1656+12_1656+19dup
XM_011537881.1:c.1656+12_1656+19dup XP_011536183.1:n.1656+12_1656+19dup
XM_011537882.1:c.1656+12_1656+19dup XP_011536184.1:n.1656+12_1656+19dup
XM_005268629.4:c.1656+12_1656+19dup XP_005268686.1:n.1656+12_1656+19dup
XM_011537877.3:c.1656+12_1656+19dup XP_011536179.1:n.1656+12_1656+19dup
XM_011537881.3:c.1656+12_1656+19dup XP_011536183.1:n.1656+12_1656+19dup
XM_011537882.3:c.1656+12_1656+19dup XP_011536184.1:n.1656+12_1656+19dup
XM_017018786.2:c.1656+12_1656+19dup XP_016874275.1:n.1656+12_1656+19dup
XM_017018789.2:c.1656+12_1656+19dup XP_016874278.1:n.1656+12_1656+19dup
XM_024448833.1:c.453+12_453+19dup XP_024304601.1:n.453+12_453+19dup
XR_001748574.2:n.1898+12_1898+19dup
NM_198578.4:c.1656+12_1656+19dup MANE Select NP_940980.4:n.1656+12_1656+19dup