Canonical Allele Identifier: CA2031025468

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363300_40363302delinsAAT , CM000674.2:g.40363300_40363302delinsAAT	GRCh38
NC_000012.11:g.40757102_40757104delinsAAT , CM000674.1:g.40757102_40757104delinsAAT	GRCh37
NC_000012.10:g.39043369_39043371delinsAAT	NCBI36
NG_011709.1:g.143290_143292delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-102_7029-100delinsAAT MANE Select	ENSP00000298910.7:n.7029-102_7029-100delinsAAT
ENST00000636518.1:c.826-102_826-100delinsAAT
ENST00000679360.1:c.*5938-102_*5938-100delinsAAT	ENSP00000505368.1:n.*5938-102_*5938-100delinsAAT
ENST00000679532.1:c.2803-102_2803-100delinsAAT
ENST00000679683.1:c.819-102_819-100delinsAAT
ENST00000680018.1:c.2474-102_2474-100delinsAAT	ENSP00000505347.1:n.2474-102_2474-100delinsAAT
ENST00000680422.1:c.4116-102_4116-100delinsAAT
ENST00000680425.1:c.2196-102_2196-100delinsAAT	ENSP00000506459.1:n.2196-102_2196-100delinsAAT
ENST00000680453.1:c.2486-102_2486-100delinsAAT
ENST00000680790.1:c.6774-102_6774-100delinsAAT	ENSP00000505335.1:n.6774-102_6774-100delinsAAT
ENST00000681136.1:n.3013-102_3013-100delinsAAT
ENST00000681696.1:c.2712-102_2712-100delinsAAT	ENSP00000505871.1:n.2712-102_2712-100delinsAAT
ENST00000681773.1:n.236-102_236-100delinsAAT
ENST00000298910.11:c.7029-102_7029-100delinsAAT	ENSP00000298910.7:n.7029-102_7029-100delinsAAT
ENST00000430804.5:c.4325-102_4325-100delinsAAT
ENST00000479187.5:n.3710-102_3710-100delinsAAT
NM_198578.3:c.7029-102_7029-100delinsAAT	NP_940980.3:n.7029-102_7029-100delinsAAT
XM_005268629.2:c.7029-102_7029-100delinsAAT	XP_005268686.1:n.7029-102_7029-100delinsAAT
XM_011537877.1:c.7029-102_7029-100delinsAAT	XP_011536179.1:n.7029-102_7029-100delinsAAT
XM_011537878.1:c.*775_*777delinsAAT	XP_011536180.1:n.*775_*777delinsAAT
XM_011537879.1:c.5826-102_5826-100delinsAAT	XP_011536181.1:n.5826-102_5826-100delinsAAT
XR_944868.1:n.485-8475_485-8473delinsATT
XM_005268629.4:c.7029-102_7029-100delinsAAT	XP_005268686.1:n.7029-102_7029-100delinsAAT
XM_011537877.3:c.7029-102_7029-100delinsAAT	XP_011536179.1:n.7029-102_7029-100delinsAAT
XM_017018787.1:c.3945-102_3945-100delinsAAT	XP_016874276.1:n.3945-102_3945-100delinsAAT
XM_017018788.2:c.3291-102_3291-100delinsAAT	XP_016874277.1:n.3291-102_3291-100delinsAAT
XM_024448833.1:c.5826-102_5826-100delinsAAT	XP_024304601.1:n.5826-102_5826-100delinsAAT
XR_944868.2:n.485-8475_485-8473delinsATT
NM_198578.4:c.7029-102_7029-100delinsAAT MANE Select	NP_940980.4:n.7029-102_7029-100delinsAAT