Canonical Allele Identifier: CA946844430

Gene: LRRK2

Linked Data

• dbSNP Id: rs1944482037
• gnomAD v3: 12-40298779-A-ATATATATATATATATG
• gnomAD v4: 12-40298779-A-ATATATATATATATATG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298794_40298795insGTATATATATATATAT , CM000674.2:g.40298794_40298795insGTATATATATATATAT	GRCh38
NC_000012.11:g.40692596_40692597insGTATATATATATATAT , CM000674.1:g.40692596_40692597insGTATATATATATATAT	GRCh37
NC_000012.10:g.38978863_38978864insGTATATATATATATAT	NCBI36
NG_011709.1:g.78784_78785insGTATATATATATATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3347+301_3347+302insGTATATATATATATAT MANE Select	ENSP00000298910.7:n.3347+301_3347+302insGTATATATATATATAT
ENST00000679360.1:c.*2256+301_*2256+302insGTATATATATATATAT	ENSP00000505368.1:n.*2256+301_*2256+302insGTATATATATATATAT
ENST00000680790.1:c.3092+301_3092+302insGTATATATATATATAT	ENSP00000505335.1:n.3092+301_3092+302insGTATATATATATATAT
ENST00000298910.11:c.3347+301_3347+302insGTATATATATATATAT	ENSP00000298910.7:n.3347+301_3347+302insGTATATATATATATAT
ENST00000343742.6:c.3347+301_3347+302insGTATATATATATATAT	ENSP00000341930.2:n.3347+301_3347+302insGTATATATATATATAT
ENST00000430804.5:c.391+301_391+302insGTATATATATATATAT
ENST00000479187.5:n.28+301_28+302insGTATATATATATATAT
NM_198578.3:c.3347+301_3347+302insGTATATATATATATAT	NP_940980.3:n.3347+301_3347+302insGTATATATATATATAT
XM_005268629.2:c.3347+301_3347+302insGTATATATATATATAT	XP_005268686.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537877.1:c.3347+301_3347+302insGTATATATATATATAT	XP_011536179.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537878.1:c.3347+301_3347+302insGTATATATATATATAT	XP_011536180.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537879.1:c.2144+301_2144+302insGTATATATATATATAT	XP_011536181.1:n.2144+301_2144+302insGTATATATATATATAT
XM_011537880.1:c.3347+301_3347+302insGTATATATATATATAT	XP_011536182.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537881.1:c.3347+301_3347+302insGTATATATATATATAT	XP_011536183.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537882.1:c.3347+301_3347+302insGTATATATATATATAT	XP_011536184.1:n.3347+301_3347+302insGTATATATATATATAT
XM_005268629.4:c.3347+301_3347+302insGTATATATATATATAT	XP_005268686.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537877.3:c.3347+301_3347+302insGTATATATATATATAT	XP_011536179.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537881.3:c.3347+301_3347+302insGTATATATATATATAT	XP_011536183.1:n.3347+301_3347+302insGTATATATATATATAT
XM_011537882.3:c.3347+301_3347+302insGTATATATATATATAT	XP_011536184.1:n.3347+301_3347+302insGTATATATATATATAT
XM_017018786.2:c.3347+301_3347+302insGTATATATATATATAT	XP_016874275.1:n.3347+301_3347+302insGTATATATATATATAT
XM_017018787.1:c.263+301_263+302insGTATATATATATATAT	XP_016874276.1:n.263+301_263+302insGTATATATATATATAT
XM_017018789.2:c.3347+301_3347+302insGTATATATATATATAT	XP_016874278.1:n.3347+301_3347+302insGTATATATATATATAT
XM_024448833.1:c.2144+301_2144+302insGTATATATATATATAT	XP_024304601.1:n.2144+301_2144+302insGTATATATATATATAT
XR_001748574.2:n.3589+301_3589+302insGTATATATATATATAT
NM_198578.4:c.3347+301_3347+302insGTATATATATATATAT MANE Select	NP_940980.4:n.3347+301_3347+302insGTATATATATATATAT