Canonical Allele Identifier: CA2618286384

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40363314-A-ATGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363315_40363316insGCCT , CM000674.2:g.40363315_40363316insGCCT	GRCh38
NC_000012.11:g.40757117_40757118insGCCT , CM000674.1:g.40757117_40757118insGCCT	GRCh37
NC_000012.10:g.39043384_39043385insGCCT	NCBI36
NG_011709.1:g.143305_143306insGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-87_7029-86insGCCT MANE Select	ENSP00000298910.7:n.7029-87_7029-86insGCCT
ENST00000636518.1:c.826-87_826-86insGCCT
ENST00000679360.1:c.*5938-87_*5938-86insGCCT	ENSP00000505368.1:n.*5938-87_*5938-86insGCCT
ENST00000679532.1:c.2803-87_2803-86insGCCT
ENST00000679683.1:c.819-87_819-86insGCCT
ENST00000680018.1:c.2474-87_2474-86insGCCT	ENSP00000505347.1:n.2474-87_2474-86insGCCT
ENST00000680422.1:c.4116-87_4116-86insGCCT
ENST00000680425.1:c.2196-87_2196-86insGCCT	ENSP00000506459.1:n.2196-87_2196-86insGCCT
ENST00000680453.1:c.2486-87_2486-86insGCCT
ENST00000680790.1:c.6774-87_6774-86insGCCT	ENSP00000505335.1:n.6774-87_6774-86insGCCT
ENST00000681136.1:n.3013-87_3013-86insGCCT
ENST00000681696.1:c.2712-87_2712-86insGCCT	ENSP00000505871.1:n.2712-87_2712-86insGCCT
ENST00000681773.1:n.236-87_236-86insGCCT
ENST00000298910.11:c.7029-87_7029-86insGCCT	ENSP00000298910.7:n.7029-87_7029-86insGCCT
ENST00000430804.5:c.4325-87_4325-86insGCCT
ENST00000479187.5:n.3710-87_3710-86insGCCT
NM_198578.3:c.7029-87_7029-86insGCCT	NP_940980.3:n.7029-87_7029-86insGCCT
XM_005268629.2:c.7029-87_7029-86insGCCT	XP_005268686.1:n.7029-87_7029-86insGCCT
XM_011537877.1:c.7029-87_7029-86insGCCT	XP_011536179.1:n.7029-87_7029-86insGCCT
XM_011537878.1:c.*790_*791insGCCT	XP_011536180.1:n.*790_*791insGCCT
XM_011537879.1:c.5826-87_5826-86insGCCT	XP_011536181.1:n.5826-87_5826-86insGCCT
XR_944868.1:n.485-8488_485-8487insGGCA
XM_005268629.4:c.7029-87_7029-86insGCCT	XP_005268686.1:n.7029-87_7029-86insGCCT
XM_011537877.3:c.7029-87_7029-86insGCCT	XP_011536179.1:n.7029-87_7029-86insGCCT
XM_017018787.1:c.3945-87_3945-86insGCCT	XP_016874276.1:n.3945-87_3945-86insGCCT
XM_017018788.2:c.3291-87_3291-86insGCCT	XP_016874277.1:n.3291-87_3291-86insGCCT
XM_024448833.1:c.5826-87_5826-86insGCCT	XP_024304601.1:n.5826-87_5826-86insGCCT
XR_944868.2:n.485-8488_485-8487insGGCA
NM_198578.4:c.7029-87_7029-86insGCCT MANE Select	NP_940980.4:n.7029-87_7029-86insGCCT