Canonical Allele Identifier: CA2031001053

Gene: LRRK2

Linked Data

• dbSNP Id: rs1945448453
• gnomAD v4: 12-40323076-CATT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323080_40323082del , CM000674.2:g.40323080_40323082del	GRCh38
NC_000012.11:g.40716882_40716884del , CM000674.1:g.40716882_40716884del	GRCh37
NC_000012.10:g.39003149_39003151del	NCBI36
NG_011709.1:g.103070_103072del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5510-80_5510-78del MANE Select	ENSP00000298910.7:n.5510-80_5510-78del
ENST00000679360.1:c.*4419-80_*4419-78del	ENSP00000505368.1:n.*4419-80_*4419-78del
ENST00000679532.1:c.1284-80_1284-78del
ENST00000680018.1:c.955-80_955-78del	ENSP00000505347.1:n.955-80_955-78del
ENST00000680422.1:c.1155-80_1155-78del
ENST00000680425.1:c.677-80_677-78del	ENSP00000506459.1:n.677-80_677-78del
ENST00000680453.1:c.967-80_967-78del
ENST00000680790.1:c.5255-80_5255-78del	ENSP00000505335.1:n.5255-80_5255-78del
ENST00000681136.1:n.1494-80_1494-78del
ENST00000681696.1:c.1193-80_1193-78del	ENSP00000505871.1:n.1193-80_1193-78del
ENST00000298910.11:c.5510-80_5510-78del	ENSP00000298910.7:n.5510-80_5510-78del
ENST00000430804.5:c.2806-80_2806-78del
ENST00000479187.5:n.2191-80_2191-78del
NM_198578.3:c.5510-80_5510-78del	NP_940980.3:n.5510-80_5510-78del
XM_005268629.2:c.5510-80_5510-78del	XP_005268686.1:n.5510-80_5510-78del
XM_011537877.1:c.5510-80_5510-78del	XP_011536179.1:n.5510-80_5510-78del
XM_011537878.1:c.5510-80_5510-78del	XP_011536180.1:n.5510-80_5510-78del
XM_011537879.1:c.4307-80_4307-78del	XP_011536181.1:n.4307-80_4307-78del
XM_005268629.4:c.5510-80_5510-78del	XP_005268686.1:n.5510-80_5510-78del
XM_011537877.3:c.5510-80_5510-78del	XP_011536179.1:n.5510-80_5510-78del
XM_017018787.1:c.2426-80_2426-78del	XP_016874276.1:n.2426-80_2426-78del
XM_017018788.2:c.1772-80_1772-78del	XP_016874277.1:n.1772-80_1772-78del
XM_024448833.1:c.4307-80_4307-78del	XP_024304601.1:n.4307-80_4307-78del
NM_198578.4:c.5510-80_5510-78del MANE Select	NP_940980.4:n.5510-80_5510-78del