Canonical Allele Identifier: CA2030983239

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298855_40298857delinsCCT , CM000674.2:g.40298855_40298857delinsCCT	GRCh38
NC_000012.11:g.40692657_40692659delinsCCT , CM000674.1:g.40692657_40692659delinsCCT	GRCh37
NC_000012.10:g.38978924_38978926delinsCCT	NCBI36
NG_011709.1:g.78845_78847delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3348-254_3348-252delinsCCT MANE Select	ENSP00000298910.7:n.3348-254_3348-252delinsCCT
ENST00000679360.1:c.*2257-254_*2257-252delinsCCT	ENSP00000505368.1:n.*2257-254_*2257-252delinsCCT
ENST00000680790.1:c.3093-254_3093-252delinsCCT	ENSP00000505335.1:n.3093-254_3093-252delinsCCT
ENST00000298910.11:c.3348-254_3348-252delinsCCT	ENSP00000298910.7:n.3348-254_3348-252delinsCCT
ENST00000343742.6:c.3348-254_3348-252delinsCCT	ENSP00000341930.2:n.3348-254_3348-252delinsCCT
ENST00000430804.5:c.392-254_392-252delinsCCT
ENST00000479187.5:n.29-254_29-252delinsCCT
NM_198578.3:c.3348-254_3348-252delinsCCT	NP_940980.3:n.3348-254_3348-252delinsCCT
XM_005268629.2:c.3348-254_3348-252delinsCCT	XP_005268686.1:n.3348-254_3348-252delinsCCT
XM_011537877.1:c.3348-254_3348-252delinsCCT	XP_011536179.1:n.3348-254_3348-252delinsCCT
XM_011537878.1:c.3348-254_3348-252delinsCCT	XP_011536180.1:n.3348-254_3348-252delinsCCT
XM_011537879.1:c.2145-254_2145-252delinsCCT	XP_011536181.1:n.2145-254_2145-252delinsCCT
XM_011537880.1:c.3348-254_3348-252delinsCCT	XP_011536182.1:n.3348-254_3348-252delinsCCT
XM_011537881.1:c.3348-254_3348-252delinsCCT	XP_011536183.1:n.3348-254_3348-252delinsCCT
XM_011537882.1:c.3348-254_3348-252delinsCCT	XP_011536184.1:n.3348-254_3348-252delinsCCT
XM_005268629.4:c.3348-254_3348-252delinsCCT	XP_005268686.1:n.3348-254_3348-252delinsCCT
XM_011537877.3:c.3348-254_3348-252delinsCCT	XP_011536179.1:n.3348-254_3348-252delinsCCT
XM_011537881.3:c.3348-254_3348-252delinsCCT	XP_011536183.1:n.3348-254_3348-252delinsCCT
XM_011537882.3:c.3348-254_3348-252delinsCCT	XP_011536184.1:n.3348-254_3348-252delinsCCT
XM_017018786.2:c.3348-254_3348-252delinsCCT	XP_016874275.1:n.3348-254_3348-252delinsCCT
XM_017018787.1:c.264-254_264-252delinsCCT	XP_016874276.1:n.264-254_264-252delinsCCT
XM_017018789.2:c.3348-254_3348-252delinsCCT	XP_016874278.1:n.3348-254_3348-252delinsCCT
XM_024448833.1:c.2145-254_2145-252delinsCCT	XP_024304601.1:n.2145-254_2145-252delinsCCT
XR_001748574.2:n.3590-254_3590-252delinsCCT
NM_198578.4:c.3348-254_3348-252delinsCCT MANE Select	NP_940980.4:n.3348-254_3348-252delinsCCT