Canonical Allele Identifier: CA2031000089
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40351564A= , CM000674.2:g.40351564A= GRCh38
NC_000012.11:g.40745366A= , CM000674.1:g.40745366A= GRCh37
NC_000012.10:g.39031633A= NCBI36
NG_011709.1:g.131554A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.6407A= MANE Select ENSP00000298910.7:p.Glu2136=
ENST00000636518.1:c.204A=
ENST00000679360.1:c.*5316A= ENSP00000505368.1:n.*5316A=
ENST00000679532.1:c.2181A=
ENST00000679683.1:c.197A=
ENST00000680018.1:c.1852A= ENSP00000505347.1:n.1852A=
ENST00000680422.1:c.2052A=
ENST00000680425.1:c.1574A= ENSP00000506459.1:n.1574A=
ENST00000680453.1:c.1864A=
ENST00000680790.1:c.6152A= ENSP00000505335.1:p.Glu2051=
ENST00000681136.1:n.2391A=
ENST00000681696.1:c.2090A= ENSP00000505871.1:p.Glu697=
ENST00000298910.11:c.6407A= ENSP00000298910.7:p.Glu2136=
ENST00000430804.5:c.3703A=
ENST00000479187.5:n.3088A=
NM_198578.3:c.6407A= NP_940980.3:p.Glu2136=
XM_005268629.2:c.6407A= XP_005268686.1:p.Glu2136=
XM_011537877.1:c.6407A= XP_011536179.1:p.Glu2136=
XM_011537878.1:c.6407A= XP_011536180.1:p.Glu2136=
XM_011537879.1:c.5204A= XP_011536181.1:p.Glu1735=
XM_005268629.4:c.6407A= XP_005268686.1:p.Glu2136=
XM_011537877.3:c.6407A= XP_011536179.1:p.Glu2136=
XM_017018787.1:c.3323A= XP_016874276.1:p.Glu1108=
XM_017018788.2:c.2669A= XP_016874277.1:p.Glu890=
XM_024448833.1:c.5204A= XP_024304601.1:p.Glu1735=
NM_198578.4:c.6407A= MANE Select NP_940980.4:p.Glu2136=