Canonical Allele Identifier: CA2515072330

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320285_40320286insATAGACTACAG , CM000674.2:g.40320285_40320286insATAGACTACAG	GRCh38
NC_000012.11:g.40714087_40714088insATAGACTACAG , CM000674.1:g.40714087_40714088insATAGACTACAG	GRCh37
NC_000012.10:g.39000354_39000355insATAGACTACAG	NCBI36
NG_011709.1:g.100275_100276insATAGACTACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+110_5015+111insATAGACTACAG MANE Select	ENSP00000298910.7:n.5015+110_5015+111insATAGACTACAG
ENST00000679360.1:c.*3924+110_*3924+111insATAGACTACAG	ENSP00000505368.1:n.*3924+110_*3924+111insATAGACTACAG
ENST00000679532.1:c.789+110_789+111insATAGACTACAG
ENST00000680018.1:c.460+110_460+111insATAGACTACAG	ENSP00000505347.1:n.460+110_460+111insATAGACTACAG
ENST00000680422.1:c.660+110_660+111insATAGACTACAG
ENST00000680425.1:c.183-749_183-748insATAGACTACAG	ENSP00000506459.1:n.183-749_183-748insATAGACTACAG
ENST00000680453.1:c.473-749_473-748insATAGACTACAG
ENST00000680790.1:c.4760+110_4760+111insATAGACTACAG	ENSP00000505335.1:n.4760+110_4760+111insATAGACTACAG
ENST00000681136.1:n.999+110_999+111insATAGACTACAG
ENST00000681696.1:c.698+110_698+111insATAGACTACAG	ENSP00000505871.1:n.698+110_698+111insATAGACTACAG
ENST00000298910.11:c.5015+110_5015+111insATAGACTACAG	ENSP00000298910.7:n.5015+110_5015+111insATAGACTACAG
ENST00000430804.5:c.2311+110_2311+111insATAGACTACAG
ENST00000479187.5:n.1696+110_1696+111insATAGACTACAG
NM_198578.3:c.5015+110_5015+111insATAGACTACAG	NP_940980.3:n.5015+110_5015+111insATAGACTACAG
XM_005268629.2:c.5015+110_5015+111insATAGACTACAG	XP_005268686.1:n.5015+110_5015+111insATAGACTACAG
XM_011537877.1:c.5015+110_5015+111insATAGACTACAG	XP_011536179.1:n.5015+110_5015+111insATAGACTACAG
XM_011537878.1:c.5015+110_5015+111insATAGACTACAG	XP_011536180.1:n.5015+110_5015+111insATAGACTACAG
XM_011537879.1:c.3812+110_3812+111insATAGACTACAG	XP_011536181.1:n.3812+110_3812+111insATAGACTACAG
XM_011537881.1:c.4828-749_4828-748insATAGACTACAG	XP_011536183.1:n.4828-749_4828-748insATAGACTACAG
XM_005268629.4:c.5015+110_5015+111insATAGACTACAG	XP_005268686.1:n.5015+110_5015+111insATAGACTACAG
XM_011537877.3:c.5015+110_5015+111insATAGACTACAG	XP_011536179.1:n.5015+110_5015+111insATAGACTACAG
XM_011537881.3:c.4828-749_4828-748insATAGACTACAG	XP_011536183.1:n.4828-749_4828-748insATAGACTACAG
XM_017018787.1:c.1931+110_1931+111insATAGACTACAG	XP_016874276.1:n.1931+110_1931+111insATAGACTACAG
XM_017018788.2:c.1277+110_1277+111insATAGACTACAG	XP_016874277.1:n.1277+110_1277+111insATAGACTACAG
XM_024448833.1:c.3812+110_3812+111insATAGACTACAG	XP_024304601.1:n.3812+110_3812+111insATAGACTACAG
XR_001748574.2:n.5383+110_5383+111insATAGACTACAG
NM_198578.4:c.5015+110_5015+111insATAGACTACAG MANE Select	NP_940980.4:n.5015+110_5015+111insATAGACTACAG