Canonical Allele Identifier: CA2726258871

Gene: LRRK2

Linked Data

• dbSNP Id: rs2136880633

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320153_40320155del , CM000674.2:g.40320153_40320155del	GRCh38
NC_000012.11:g.40713955_40713957del , CM000674.1:g.40713955_40713957del	GRCh37
NC_000012.10:g.39000222_39000224del	NCBI36
NG_011709.1:g.100143_100145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4993_4995del MANE Select	ENSP00000298910.7:p.Glu1665del
ENST00000679360.1:c.*3902_*3904del	ENSP00000505368.1:n.*3902_*3904del
ENST00000679532.1:c.767_769del
ENST00000680018.1:c.438_440del	ENSP00000505347.1:n.438_440del
ENST00000680422.1:c.638_640del
ENST00000680425.1:c.183-881_183-879del	ENSP00000506459.1:n.183-881_183-879del
ENST00000680453.1:c.473-881_473-879del
ENST00000680790.1:c.4738_4740del	ENSP00000505335.1:p.Glu1580del
ENST00000681136.1:n.977_979del
ENST00000681696.1:c.676_678del	ENSP00000505871.1:p.Glu226del
ENST00000298910.11:c.4993_4995del	ENSP00000298910.7:p.Glu1665del
ENST00000430804.5:c.2289_2291del
ENST00000479187.5:n.1674_1676del
NM_198578.3:c.4993_4995del	NP_940980.3:p.Glu1665del
XM_005268629.2:c.4993_4995del	XP_005268686.1:p.Glu1665del
XM_011537877.1:c.4993_4995del	XP_011536179.1:p.Glu1665del
XM_011537878.1:c.4993_4995del	XP_011536180.1:p.Glu1665del
XM_011537879.1:c.3790_3792del	XP_011536181.1:p.Glu1264del
XM_011537881.1:c.4828-881_4828-879del	XP_011536183.1:n.4828-881_4828-879del
XM_005268629.4:c.4993_4995del	XP_005268686.1:p.Glu1665del
XM_011537877.3:c.4993_4995del	XP_011536179.1:p.Glu1665del
XM_011537881.3:c.4828-881_4828-879del	XP_011536183.1:n.4828-881_4828-879del
XM_017018787.1:c.1909_1911del	XP_016874276.1:p.Glu637del
XM_017018788.2:c.1255_1257del	XP_016874277.1:p.Glu419del
XM_024448833.1:c.3790_3792del	XP_024304601.1:p.Glu1264del
XR_001748574.2:n.5361_5363del
NM_198578.4:c.4993_4995del MANE Select	NP_940980.4:p.Glu1665del