Canonical Allele Identifier: CA2566670642

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40308864_40308865del , CM000674.2:g.40308864_40308865del	GRCh38
NC_000012.11:g.40702666_40702667del , CM000674.1:g.40702666_40702667del	GRCh37
NC_000012.10:g.38988933_38988934del	NCBI36
NG_011709.1:g.88854_88855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4189+168_4189+169del MANE Select	ENSP00000298910.7:n.4189+168_4189+169del
ENST00000679360.1:c.*3098+168_*3098+169del	ENSP00000505368.1:n.*3098+168_*3098+169del
ENST00000680790.1:c.3934+168_3934+169del	ENSP00000505335.1:n.3934+168_3934+169del
ENST00000298910.11:c.4189+168_4189+169del	ENSP00000298910.7:n.4189+168_4189+169del
ENST00000430804.5:c.1485+168_1485+169del
ENST00000479187.5:n.870+168_870+169del
NM_198578.3:c.4189+168_4189+169del	NP_940980.3:n.4189+168_4189+169del
XM_005268629.2:c.4189+168_4189+169del	XP_005268686.1:n.4189+168_4189+169del
XM_011537877.1:c.4189+168_4189+169del	XP_011536179.1:n.4189+168_4189+169del
XM_011537878.1:c.4189+168_4189+169del	XP_011536180.1:n.4189+168_4189+169del
XM_011537879.1:c.2986+168_2986+169del	XP_011536181.1:n.2986+168_2986+169del
XM_011537880.1:c.4189+168_4189+169del	XP_011536182.1:n.4189+168_4189+169del
XM_011537881.1:c.4189+168_4189+169del	XP_011536183.1:n.4189+168_4189+169del
XM_005268629.4:c.4189+168_4189+169del	XP_005268686.1:n.4189+168_4189+169del
XM_011537877.3:c.4189+168_4189+169del	XP_011536179.1:n.4189+168_4189+169del
XM_011537881.3:c.4189+168_4189+169del	XP_011536183.1:n.4189+168_4189+169del
XM_017018786.2:c.4189+168_4189+169del	XP_016874275.1:n.4189+168_4189+169del
XM_017018787.1:c.1105+168_1105+169del	XP_016874276.1:n.1105+168_1105+169del
XM_017018788.2:c.451+168_451+169del	XP_016874277.1:n.451+168_451+169del
XM_024448833.1:c.2986+168_2986+169del	XP_024304601.1:n.2986+168_2986+169del
XR_001748574.2:n.4431+168_4431+169del
NM_198578.4:c.4189+168_4189+169del MANE Select	NP_940980.4:n.4189+168_4189+169del