Canonical Allele Identifier: CA2575122361
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363537_40363540del , CM000674.2:g.40363537_40363540del GRCh38
NC_000012.11:g.40757339_40757342del , CM000674.1:g.40757339_40757342del GRCh37
NC_000012.10:g.39043606_39043609del NCBI36
NG_011709.1:g.143527_143530del

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7164_7167del MANE Select ENSP00000298910.7:p.Asp2388GlufsTer5
ENST00000636518.1:c.961_964del
ENST00000679360.1:c.*6073_*6076del ENSP00000505368.1:n.*6073_*6076del
ENST00000679532.1:c.2938_2941del
ENST00000679683.1:c.954_957del
ENST00000680018.1:c.2609_2612del ENSP00000505347.1:n.2609_2612del
ENST00000680422.1:c.4251_4254del
ENST00000680425.1:c.2331_2334del ENSP00000506459.1:n.2331_2334del
ENST00000680453.1:c.2621_2624del
ENST00000680790.1:c.6909_6912del ENSP00000505335.1:p.Asp2303GlufsTer5
ENST00000681136.1:n.3148_3151del
ENST00000681696.1:c.2847_2850del ENSP00000505871.1:p.Asp949GlufsTer5
ENST00000681773.1:n.371_374del
ENST00000298910.11:c.7164_7167del ENSP00000298910.7:p.Asp2388GlufsTer5
ENST00000430804.5:c.4460_4463del
ENST00000479187.5:n.3845_3848del
NM_198578.3:c.7164_7167del NP_940980.3:p.Asp2388GlufsTer5
XM_005268629.2:c.7164_7167del XP_005268686.1:p.Asp2388GlufsTer5
XM_011537877.1:c.7164_7167del XP_011536179.1:p.Asp2388GlufsTer5
XM_011537879.1:c.5961_5964del XP_011536181.1:p.Asp1987GlufsTer5
XR_944868.1:n.485-8713_485-8710del
XM_005268629.4:c.7164_7167del XP_005268686.1:p.Asp2388GlufsTer5
XM_011537877.3:c.7164_7167del XP_011536179.1:p.Asp2388GlufsTer5
XM_017018787.1:c.4080_4083del XP_016874276.1:p.Asp1360GlufsTer5
XM_017018788.2:c.3426_3429del XP_016874277.1:p.Asp1142GlufsTer5
XM_024448833.1:c.5961_5964del XP_024304601.1:p.Asp1987GlufsTer5
XR_944868.2:n.485-8713_485-8710del
NM_198578.4:c.7164_7167del MANE Select NP_940980.4:p.Asp2388GlufsTer5