Canonical Allele Identifier: CA2030983041

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298789_40298794delinsATATAT , CM000674.2:g.40298789_40298794delinsATATAT	GRCh38
NC_000012.11:g.40692591_40692596delinsATATAT , CM000674.1:g.40692591_40692596delinsATATAT	GRCh37
NC_000012.10:g.38978858_38978863delinsATATAT	NCBI36
NG_011709.1:g.78779_78784delinsATATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3347+296_3347+301delinsATATAT MANE Select	ENSP00000298910.7:n.3347+296_3347+301delinsATATAT
ENST00000679360.1:c.*2256+296_*2256+301delinsATATAT	ENSP00000505368.1:n.*2256+296_*2256+301delinsATATAT
ENST00000680790.1:c.3092+296_3092+301delinsATATAT	ENSP00000505335.1:n.3092+296_3092+301delinsATATAT
ENST00000298910.11:c.3347+296_3347+301delinsATATAT	ENSP00000298910.7:n.3347+296_3347+301delinsATATAT
ENST00000343742.6:c.3347+296_3347+301delinsATATAT	ENSP00000341930.2:n.3347+296_3347+301delinsATATAT
ENST00000430804.5:c.391+296_391+301delinsATATAT
ENST00000479187.5:n.28+296_28+301delinsATATAT
NM_198578.3:c.3347+296_3347+301delinsATATAT	NP_940980.3:n.3347+296_3347+301delinsATATAT
XM_005268629.2:c.3347+296_3347+301delinsATATAT	XP_005268686.1:n.3347+296_3347+301delinsATATAT
XM_011537877.1:c.3347+296_3347+301delinsATATAT	XP_011536179.1:n.3347+296_3347+301delinsATATAT
XM_011537878.1:c.3347+296_3347+301delinsATATAT	XP_011536180.1:n.3347+296_3347+301delinsATATAT
XM_011537879.1:c.2144+296_2144+301delinsATATAT	XP_011536181.1:n.2144+296_2144+301delinsATATAT
XM_011537880.1:c.3347+296_3347+301delinsATATAT	XP_011536182.1:n.3347+296_3347+301delinsATATAT
XM_011537881.1:c.3347+296_3347+301delinsATATAT	XP_011536183.1:n.3347+296_3347+301delinsATATAT
XM_011537882.1:c.3347+296_3347+301delinsATATAT	XP_011536184.1:n.3347+296_3347+301delinsATATAT
XM_005268629.4:c.3347+296_3347+301delinsATATAT	XP_005268686.1:n.3347+296_3347+301delinsATATAT
XM_011537877.3:c.3347+296_3347+301delinsATATAT	XP_011536179.1:n.3347+296_3347+301delinsATATAT
XM_011537881.3:c.3347+296_3347+301delinsATATAT	XP_011536183.1:n.3347+296_3347+301delinsATATAT
XM_011537882.3:c.3347+296_3347+301delinsATATAT	XP_011536184.1:n.3347+296_3347+301delinsATATAT
XM_017018786.2:c.3347+296_3347+301delinsATATAT	XP_016874275.1:n.3347+296_3347+301delinsATATAT
XM_017018787.1:c.263+296_263+301delinsATATAT	XP_016874276.1:n.263+296_263+301delinsATATAT
XM_017018789.2:c.3347+296_3347+301delinsATATAT	XP_016874278.1:n.3347+296_3347+301delinsATATAT
XM_024448833.1:c.2144+296_2144+301delinsATATAT	XP_024304601.1:n.2144+296_2144+301delinsATATAT
XR_001748574.2:n.3589+296_3589+301delinsATATAT
NM_198578.4:c.3347+296_3347+301delinsATATAT MANE Select	NP_940980.4:n.3347+296_3347+301delinsATATAT