Canonical Allele Identifier: CA2795683182

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40321025del , CM000674.2:g.40321025del	GRCh38
NC_000012.11:g.40714827del , CM000674.1:g.40714827del	GRCh37
NC_000012.10:g.39001094del	NCBI36
NG_011709.1:g.101015del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5016-9del MANE Select	ENSP00000298910.7:n.5016-9del
ENST00000679360.1:c.*3925-9del	ENSP00000505368.1:n.*3925-9del
ENST00000679532.1:c.790-9del
ENST00000680018.1:c.461-9del	ENSP00000505347.1:n.461-9del
ENST00000680422.1:c.661-9del
ENST00000680425.1:c.183-9del	ENSP00000506459.1:n.183-9del
ENST00000680453.1:c.473-9del
ENST00000680790.1:c.4761-9del	ENSP00000505335.1:n.4761-9del
ENST00000681136.1:n.1000-9del
ENST00000681696.1:c.699-9del	ENSP00000505871.1:n.699-9del
ENST00000298910.11:c.5016-9del	ENSP00000298910.7:n.5016-9del
ENST00000430804.5:c.2312-9del
ENST00000479187.5:n.1697-9del
NM_198578.3:c.5016-9del	NP_940980.3:n.5016-9del
XM_005268629.2:c.5016-9del	XP_005268686.1:n.5016-9del
XM_011537877.1:c.5016-9del	XP_011536179.1:n.5016-9del
XM_011537878.1:c.5016-9del	XP_011536180.1:n.5016-9del
XM_011537879.1:c.3813-9del	XP_011536181.1:n.3813-9del
XM_011537881.1:c.4828-9del	XP_011536183.1:n.4828-9del
XM_005268629.4:c.5016-9del	XP_005268686.1:n.5016-9del
XM_011537877.3:c.5016-9del	XP_011536179.1:n.5016-9del
XM_011537881.3:c.4828-9del	XP_011536183.1:n.4828-9del
XM_017018787.1:c.1932-9del	XP_016874276.1:n.1932-9del
XM_017018788.2:c.1278-9del	XP_016874277.1:n.1278-9del
XM_024448833.1:c.3813-9del	XP_024304601.1:n.3813-9del
XR_001748574.2:n.5384-9del
NM_198578.4:c.5016-9del MANE Select	NP_940980.4:n.5016-9del