Canonical Allele Identifier: CA2031027685

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340672_40340675delinsAAAG , CM000674.2:g.40340672_40340675delinsAAAG	GRCh38
NC_000012.11:g.40734474_40734477delinsAAAG , CM000674.1:g.40734474_40734477delinsAAAG	GRCh37
NC_000012.10:g.39020741_39020744delinsAAAG	NCBI36
NG_011709.1:g.120662_120665delinsAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6109+218_6109+221delinsAAAG MANE Select	ENSP00000298910.7:n.6109+218_6109+221delinsAAAG
ENST00000679360.1:c.*5018+218_*5018+221delinsAAAG	ENSP00000505368.1:n.*5018+218_*5018+221delinsAAAG
ENST00000679532.1:c.1883+218_1883+221delinsAAAG
ENST00000680018.1:c.1554+218_1554+221delinsAAAG	ENSP00000505347.1:n.1554+218_1554+221delinsAAAG
ENST00000680422.1:c.1754+218_1754+221delinsAAAG
ENST00000680425.1:c.1276+218_1276+221delinsAAAG	ENSP00000506459.1:n.1276+218_1276+221delinsAAAG
ENST00000680453.1:c.1566+218_1566+221delinsAAAG
ENST00000680790.1:c.5854+218_5854+221delinsAAAG	ENSP00000505335.1:n.5854+218_5854+221delinsAAAG
ENST00000681136.1:n.2093+218_2093+221delinsAAAG
ENST00000681696.1:c.1792+218_1792+221delinsAAAG	ENSP00000505871.1:n.1792+218_1792+221delinsAAAG
ENST00000298910.11:c.6109+218_6109+221delinsAAAG	ENSP00000298910.7:n.6109+218_6109+221delinsAAAG
ENST00000430804.5:c.3405+218_3405+221delinsAAAG
ENST00000479187.5:n.2790+218_2790+221delinsAAAG
NM_198578.3:c.6109+218_6109+221delinsAAAG	NP_940980.3:n.6109+218_6109+221delinsAAAG
XM_005268629.2:c.6109+218_6109+221delinsAAAG	XP_005268686.1:n.6109+218_6109+221delinsAAAG
XM_011537877.1:c.6109+218_6109+221delinsAAAG	XP_011536179.1:n.6109+218_6109+221delinsAAAG
XM_011537878.1:c.6109+218_6109+221delinsAAAG	XP_011536180.1:n.6109+218_6109+221delinsAAAG
XM_011537879.1:c.4906+218_4906+221delinsAAAG	XP_011536181.1:n.4906+218_4906+221delinsAAAG
XM_005268629.4:c.6109+218_6109+221delinsAAAG	XP_005268686.1:n.6109+218_6109+221delinsAAAG
XM_011537877.3:c.6109+218_6109+221delinsAAAG	XP_011536179.1:n.6109+218_6109+221delinsAAAG
XM_017018787.1:c.3025+218_3025+221delinsAAAG	XP_016874276.1:n.3025+218_3025+221delinsAAAG
XM_017018788.2:c.2371+218_2371+221delinsAAAG	XP_016874277.1:n.2371+218_2371+221delinsAAAG
XM_024448833.1:c.4906+218_4906+221delinsAAAG	XP_024304601.1:n.4906+218_4906+221delinsAAAG
NM_198578.4:c.6109+218_6109+221delinsAAAG MANE Select	NP_940980.4:n.6109+218_6109+221delinsAAAG