Canonical Allele Identifier: CA2031002291

Gene: LRRK2

Linked Data

• dbSNP Id: rs1944933245

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40308952_40308956del , CM000674.2:g.40308952_40308956del	GRCh38
NC_000012.11:g.40702754_40702758del , CM000674.1:g.40702754_40702758del	GRCh37
NC_000012.10:g.38989021_38989025del	NCBI36
NG_011709.1:g.88942_88946del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4190-154_4190-150del MANE Select	ENSP00000298910.7:n.4190-154_4190-150del
ENST00000679360.1:c.*3099-154_*3099-150del	ENSP00000505368.1:n.*3099-154_*3099-150del
ENST00000680790.1:c.3935-154_3935-150del	ENSP00000505335.1:n.3935-154_3935-150del
ENST00000298910.11:c.4190-154_4190-150del	ENSP00000298910.7:n.4190-154_4190-150del
ENST00000430804.5:c.1486-154_1486-150del
ENST00000479187.5:n.871-154_871-150del
NM_198578.3:c.4190-154_4190-150del	NP_940980.3:n.4190-154_4190-150del
XM_005268629.2:c.4190-154_4190-150del	XP_005268686.1:n.4190-154_4190-150del
XM_011537877.1:c.4190-154_4190-150del	XP_011536179.1:n.4190-154_4190-150del
XM_011537878.1:c.4190-154_4190-150del	XP_011536180.1:n.4190-154_4190-150del
XM_011537879.1:c.2987-154_2987-150del	XP_011536181.1:n.2987-154_2987-150del
XM_011537880.1:c.4190-154_4190-150del	XP_011536182.1:n.4190-154_4190-150del
XM_011537881.1:c.4190-154_4190-150del	XP_011536183.1:n.4190-154_4190-150del
XM_005268629.4:c.4190-154_4190-150del	XP_005268686.1:n.4190-154_4190-150del
XM_011537877.3:c.4190-154_4190-150del	XP_011536179.1:n.4190-154_4190-150del
XM_011537881.3:c.4190-154_4190-150del	XP_011536183.1:n.4190-154_4190-150del
XM_017018786.2:c.4190-154_4190-150del	XP_016874275.1:n.4190-154_4190-150del
XM_017018787.1:c.1106-154_1106-150del	XP_016874276.1:n.1106-154_1106-150del
XM_017018788.2:c.452-154_452-150del	XP_016874277.1:n.452-154_452-150del
XM_024448833.1:c.2987-154_2987-150del	XP_024304601.1:n.2987-154_2987-150del
XR_001748574.2:n.4432-154_4432-150del
NM_198578.4:c.4190-154_4190-150del MANE Select	NP_940980.4:n.4190-154_4190-150del