Canonical Allele Identifier: CA2977668514
Gene: LRRK2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.7164del MANE Select ENSP00000298910.7:p.Cys2389AlafsTer5
ENST00000636518.1:c.961del
ENST00000679360.1:c.*6073del ENSP00000505368.1:n.*6073del
ENST00000679532.1:c.2938del
ENST00000679683.1:c.954del
ENST00000680018.1:c.2609del ENSP00000505347.1:n.2609del
ENST00000680422.1:c.4251del
ENST00000680425.1:c.2331del ENSP00000506459.1:n.2331del
ENST00000680453.1:c.2621del
ENST00000680790.1:c.6909del ENSP00000505335.1:p.Cys2304AlafsTer5
ENST00000681136.1:n.3148del
ENST00000681696.1:c.2847del ENSP00000505871.1:p.Cys950AlafsTer5
ENST00000681773.1:n.371del
ENST00000298910.11:c.7164del ENSP00000298910.7:p.Cys2389AlafsTer5
ENST00000430804.5:c.4460del
ENST00000479187.5:n.3845del
NM_198578.3:c.7164del NP_940980.3:p.Cys2389AlafsTer5
XM_005268629.2:c.7164del XP_005268686.1:p.Cys2389AlafsTer5
XM_011537877.1:c.7164del XP_011536179.1:p.Cys2389AlafsTer5
XM_011537879.1:c.5961del XP_011536181.1:p.Cys1988AlafsTer5
XR_944868.1:n.485-8710del
XM_005268629.4:c.7164del XP_005268686.1:p.Cys2389AlafsTer5
XM_011537877.3:c.7164del XP_011536179.1:p.Cys2389AlafsTer5
XM_017018787.1:c.4080del XP_016874276.1:p.Cys1361AlafsTer5
XM_017018788.2:c.3426del XP_016874277.1:p.Cys1143AlafsTer5
XM_024448833.1:c.5961del XP_024304601.1:p.Cys1988AlafsTer5
XR_944868.2:n.485-8710del
NM_198578.4:c.7164del MANE Select NP_940980.4:p.Cys2389AlafsTer5