Canonical Allele Identifier: CA2031027496

Gene: LRRK2

Linked Data

• dbSNP Id: rs1946008281
• gnomAD v4: 12-40340532-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340536del , CM000674.2:g.40340536del	GRCh38
NC_000012.11:g.40734338del , CM000674.1:g.40734338del	GRCh37
NC_000012.10:g.39020605del	NCBI36
NG_011709.1:g.120526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6109+82del MANE Select	ENSP00000298910.7:n.6109+82del
ENST00000679360.1:c.*5018+82del	ENSP00000505368.1:n.*5018+82del
ENST00000679532.1:c.1883+82del
ENST00000680018.1:c.1554+82del	ENSP00000505347.1:n.1554+82del
ENST00000680422.1:c.1754+82del
ENST00000680425.1:c.1276+82del	ENSP00000506459.1:n.1276+82del
ENST00000680453.1:c.1566+82del
ENST00000680790.1:c.5854+82del	ENSP00000505335.1:n.5854+82del
ENST00000681136.1:n.2093+82del
ENST00000681696.1:c.1792+82del	ENSP00000505871.1:n.1792+82del
ENST00000298910.11:c.6109+82del	ENSP00000298910.7:n.6109+82del
ENST00000430804.5:c.3405+82del
ENST00000479187.5:n.2790+82del
NM_198578.3:c.6109+82del	NP_940980.3:n.6109+82del
XM_005268629.2:c.6109+82del	XP_005268686.1:n.6109+82del
XM_011537877.1:c.6109+82del	XP_011536179.1:n.6109+82del
XM_011537878.1:c.6109+82del	XP_011536180.1:n.6109+82del
XM_011537879.1:c.4906+82del	XP_011536181.1:n.4906+82del
XM_005268629.4:c.6109+82del	XP_005268686.1:n.6109+82del
XM_011537877.3:c.6109+82del	XP_011536179.1:n.6109+82del
XM_017018787.1:c.3025+82del	XP_016874276.1:n.3025+82del
XM_017018788.2:c.2371+82del	XP_016874277.1:n.2371+82del
XM_024448833.1:c.4906+82del	XP_024304601.1:n.4906+82del
NM_198578.4:c.6109+82del MANE Select	NP_940980.4:n.6109+82del