Canonical Allele Identifier: CA2030982899

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298575_40298576delinsGA , CM000674.2:g.40298575_40298576delinsGA	GRCh38
NC_000012.11:g.40692377_40692378delinsGA , CM000674.1:g.40692377_40692378delinsGA	GRCh37
NC_000012.10:g.38978644_38978645delinsGA	NCBI36
NG_011709.1:g.78565_78566delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3347+82_3347+83delinsGA MANE Select	ENSP00000298910.7:n.3347+82_3347+83delinsGA
ENST00000679360.1:c.*2256+82_*2256+83delinsGA	ENSP00000505368.1:n.*2256+82_*2256+83delinsGA
ENST00000680790.1:c.3092+82_3092+83delinsGA	ENSP00000505335.1:n.3092+82_3092+83delinsGA
ENST00000298910.11:c.3347+82_3347+83delinsGA	ENSP00000298910.7:n.3347+82_3347+83delinsGA
ENST00000343742.6:c.3347+82_3347+83delinsGA	ENSP00000341930.2:n.3347+82_3347+83delinsGA
ENST00000430804.5:c.391+82_391+83delinsGA
ENST00000479187.5:n.28+82_28+83delinsGA
NM_198578.3:c.3347+82_3347+83delinsGA	NP_940980.3:n.3347+82_3347+83delinsGA
XM_005268629.2:c.3347+82_3347+83delinsGA	XP_005268686.1:n.3347+82_3347+83delinsGA
XM_011537877.1:c.3347+82_3347+83delinsGA	XP_011536179.1:n.3347+82_3347+83delinsGA
XM_011537878.1:c.3347+82_3347+83delinsGA	XP_011536180.1:n.3347+82_3347+83delinsGA
XM_011537879.1:c.2144+82_2144+83delinsGA	XP_011536181.1:n.2144+82_2144+83delinsGA
XM_011537880.1:c.3347+82_3347+83delinsGA	XP_011536182.1:n.3347+82_3347+83delinsGA
XM_011537881.1:c.3347+82_3347+83delinsGA	XP_011536183.1:n.3347+82_3347+83delinsGA
XM_011537882.1:c.3347+82_3347+83delinsGA	XP_011536184.1:n.3347+82_3347+83delinsGA
XM_005268629.4:c.3347+82_3347+83delinsGA	XP_005268686.1:n.3347+82_3347+83delinsGA
XM_011537877.3:c.3347+82_3347+83delinsGA	XP_011536179.1:n.3347+82_3347+83delinsGA
XM_011537881.3:c.3347+82_3347+83delinsGA	XP_011536183.1:n.3347+82_3347+83delinsGA
XM_011537882.3:c.3347+82_3347+83delinsGA	XP_011536184.1:n.3347+82_3347+83delinsGA
XM_017018786.2:c.3347+82_3347+83delinsGA	XP_016874275.1:n.3347+82_3347+83delinsGA
XM_017018787.1:c.263+82_263+83delinsGA	XP_016874276.1:n.263+82_263+83delinsGA
XM_017018789.2:c.3347+82_3347+83delinsGA	XP_016874278.1:n.3347+82_3347+83delinsGA
XM_024448833.1:c.2144+82_2144+83delinsGA	XP_024304601.1:n.2144+82_2144+83delinsGA
XR_001748574.2:n.3589+82_3589+83delinsGA
NM_198578.4:c.3347+82_3347+83delinsGA MANE Select	NP_940980.4:n.3347+82_3347+83delinsGA