Canonical Allele Identifier: CA384409525

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40252984C>G , CM000674.2:g.40252984C>G	GRCh38
NC_000012.11:g.40646786C>G , CM000674.1:g.40646786C>G	GRCh37
NC_000012.10:g.38933053C>G	NCBI36
NG_011709.1:g.32974C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.1256C>G MANE Select	NP_940980.4:p.Ala419Gly
ENST00000298910.12:c.1256C>G MANE Select	ENSP00000298910.7:p.Ala419Gly
NM_198578.3:c.1256C>G	NP_940980.3:p.Ala419Gly
ENST00000298910.11:c.1256C>G	ENSP00000298910.7:p.Ala419Gly
ENST00000343742.6:c.1256C>G	ENSP00000341930.2:p.Ala419Gly
ENST00000416796.5:c.630C>G	ENSP00000398726.1:p.Cys210Trp
ENST00000679360.1:c.*165C>G	ENSP00000505368.1:n.*165C>G
ENST00000680790.1:c.1256C>G	ENSP00000505335.1:p.Ala419Gly
XM_005268629.2:c.1256C>G	XP_005268686.1:p.Ala419Gly
XM_005268629.4:c.1256C>G	XP_005268686.1:p.Ala419Gly
XM_011537877.1:c.1256C>G	XP_011536179.1:p.Ala419Gly
XM_011537877.3:c.1256C>G	XP_011536179.1:p.Ala419Gly
XM_011537878.1:c.1256C>G	XP_011536180.1:p.Ala419Gly
XM_011537879.1:c.53C>G	XP_011536181.1:p.Ala18Gly
XM_011537880.1:c.1256C>G	XP_011536182.1:p.Ala419Gly
XM_011537881.1:c.1256C>G	XP_011536183.1:p.Ala419Gly
XM_011537881.3:c.1256C>G	XP_011536183.1:p.Ala419Gly
XM_011537882.1:c.1256C>G	XP_011536184.1:p.Ala419Gly
XM_011537882.3:c.1256C>G	XP_011536184.1:p.Ala419Gly
XM_017018786.2:c.1256C>G	XP_016874275.1:p.Ala419Gly
XM_017018789.2:c.1256C>G	XP_016874278.1:p.Ala419Gly
XM_024448833.1:c.53C>G	XP_024304601.1:p.Ala18Gly
XR_001748574.2:n.1498C>G