Canonical Allele Identifier: CA2031002139

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40308889_40308890delinsAT , CM000674.2:g.40308889_40308890delinsAT	GRCh38
NC_000012.11:g.40702691_40702692delinsAT , CM000674.1:g.40702691_40702692delinsAT	GRCh37
NC_000012.10:g.38988958_38988959delinsAT	NCBI36
NG_011709.1:g.88879_88880delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4189+193_4189+194delinsAT MANE Select	ENSP00000298910.7:n.4189+193_4189+194delinsAT
ENST00000679360.1:c.*3098+193_*3098+194delinsAT	ENSP00000505368.1:n.*3098+193_*3098+194delinsAT
ENST00000680790.1:c.3934+193_3934+194delinsAT	ENSP00000505335.1:n.3934+193_3934+194delinsAT
ENST00000298910.11:c.4189+193_4189+194delinsAT	ENSP00000298910.7:n.4189+193_4189+194delinsAT
ENST00000430804.5:c.1485+193_1485+194delinsAT
ENST00000479187.5:n.870+193_870+194delinsAT
NM_198578.3:c.4189+193_4189+194delinsAT	NP_940980.3:n.4189+193_4189+194delinsAT
XM_005268629.2:c.4189+193_4189+194delinsAT	XP_005268686.1:n.4189+193_4189+194delinsAT
XM_011537877.1:c.4189+193_4189+194delinsAT	XP_011536179.1:n.4189+193_4189+194delinsAT
XM_011537878.1:c.4189+193_4189+194delinsAT	XP_011536180.1:n.4189+193_4189+194delinsAT
XM_011537879.1:c.2986+193_2986+194delinsAT	XP_011536181.1:n.2986+193_2986+194delinsAT
XM_011537880.1:c.4189+193_4189+194delinsAT	XP_011536182.1:n.4189+193_4189+194delinsAT
XM_011537881.1:c.4189+193_4189+194delinsAT	XP_011536183.1:n.4189+193_4189+194delinsAT
XM_005268629.4:c.4189+193_4189+194delinsAT	XP_005268686.1:n.4189+193_4189+194delinsAT
XM_011537877.3:c.4189+193_4189+194delinsAT	XP_011536179.1:n.4189+193_4189+194delinsAT
XM_011537881.3:c.4189+193_4189+194delinsAT	XP_011536183.1:n.4189+193_4189+194delinsAT
XM_017018786.2:c.4189+193_4189+194delinsAT	XP_016874275.1:n.4189+193_4189+194delinsAT
XM_017018787.1:c.1105+193_1105+194delinsAT	XP_016874276.1:n.1105+193_1105+194delinsAT
XM_017018788.2:c.451+193_451+194delinsAT	XP_016874277.1:n.451+193_451+194delinsAT
XM_024448833.1:c.2986+193_2986+194delinsAT	XP_024304601.1:n.2986+193_2986+194delinsAT
XR_001748574.2:n.4431+193_4431+194delinsAT
NM_198578.4:c.4189+193_4189+194delinsAT MANE Select	NP_940980.4:n.4189+193_4189+194delinsAT