Canonical Allele Identifier: CA2560108932

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320329_40320330insTTAAGGTTTTCT , CM000674.2:g.40320329_40320330insTTAAGGTTTTCT	GRCh38
NC_000012.11:g.40714131_40714132insTTAAGGTTTTCT , CM000674.1:g.40714131_40714132insTTAAGGTTTTCT	GRCh37
NC_000012.10:g.39000398_39000399insTTAAGGTTTTCT	NCBI36
NG_011709.1:g.100319_100320insTTAAGGTTTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5015+154_5015+155insTTAAGGTTTTCT MANE Select	ENSP00000298910.7:n.5015+154_5015+155insTTAAGGTTTTCT
ENST00000679360.1:c.*3924+154_*3924+155insTTAAGGTTTTCT	ENSP00000505368.1:n.*3924+154_*3924+155insTTAAGGTTTTCT
ENST00000679532.1:c.789+154_789+155insTTAAGGTTTTCT
ENST00000680018.1:c.460+154_460+155insTTAAGGTTTTCT	ENSP00000505347.1:n.460+154_460+155insTTAAGGTTTTCT
ENST00000680422.1:c.660+154_660+155insTTAAGGTTTTCT
ENST00000680425.1:c.183-705_183-704insTTAAGGTTTTCT	ENSP00000506459.1:n.183-705_183-704insTTAAGGTTTTCT
ENST00000680453.1:c.473-705_473-704insTTAAGGTTTTCT
ENST00000680790.1:c.4760+154_4760+155insTTAAGGTTTTCT	ENSP00000505335.1:n.4760+154_4760+155insTTAAGGTTTTCT
ENST00000681136.1:n.999+154_999+155insTTAAGGTTTTCT
ENST00000681696.1:c.698+154_698+155insTTAAGGTTTTCT	ENSP00000505871.1:n.698+154_698+155insTTAAGGTTTTCT
ENST00000298910.11:c.5015+154_5015+155insTTAAGGTTTTCT	ENSP00000298910.7:n.5015+154_5015+155insTTAAGGTTTTCT
ENST00000430804.5:c.2311+154_2311+155insTTAAGGTTTTCT
ENST00000479187.5:n.1696+154_1696+155insTTAAGGTTTTCT
NM_198578.3:c.5015+154_5015+155insTTAAGGTTTTCT	NP_940980.3:n.5015+154_5015+155insTTAAGGTTTTCT
XM_005268629.2:c.5015+154_5015+155insTTAAGGTTTTCT	XP_005268686.1:n.5015+154_5015+155insTTAAGGTTTTCT
XM_011537877.1:c.5015+154_5015+155insTTAAGGTTTTCT	XP_011536179.1:n.5015+154_5015+155insTTAAGGTTTTCT
XM_011537878.1:c.5015+154_5015+155insTTAAGGTTTTCT	XP_011536180.1:n.5015+154_5015+155insTTAAGGTTTTCT
XM_011537879.1:c.3812+154_3812+155insTTAAGGTTTTCT	XP_011536181.1:n.3812+154_3812+155insTTAAGGTTTTCT
XM_011537881.1:c.4828-705_4828-704insTTAAGGTTTTCT	XP_011536183.1:n.4828-705_4828-704insTTAAGGTTTTCT
XM_005268629.4:c.5015+154_5015+155insTTAAGGTTTTCT	XP_005268686.1:n.5015+154_5015+155insTTAAGGTTTTCT
XM_011537877.3:c.5015+154_5015+155insTTAAGGTTTTCT	XP_011536179.1:n.5015+154_5015+155insTTAAGGTTTTCT
XM_011537881.3:c.4828-705_4828-704insTTAAGGTTTTCT	XP_011536183.1:n.4828-705_4828-704insTTAAGGTTTTCT
XM_017018787.1:c.1931+154_1931+155insTTAAGGTTTTCT	XP_016874276.1:n.1931+154_1931+155insTTAAGGTTTTCT
XM_017018788.2:c.1277+154_1277+155insTTAAGGTTTTCT	XP_016874277.1:n.1277+154_1277+155insTTAAGGTTTTCT
XM_024448833.1:c.3812+154_3812+155insTTAAGGTTTTCT	XP_024304601.1:n.3812+154_3812+155insTTAAGGTTTTCT
XR_001748574.2:n.5383+154_5383+155insTTAAGGTTTTCT
NM_198578.4:c.5015+154_5015+155insTTAAGGTTTTCT MANE Select	NP_940980.4:n.5015+154_5015+155insTTAAGGTTTTCT