Canonical Allele Identifier: CA384403492
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340301C>A , CM000674.2:g.40340301C>A GRCh38
NC_000012.11:g.40734103C>A , CM000674.1:g.40734103C>A GRCh37
NC_000012.10:g.39020370C>A NCBI36
NG_011709.1:g.120291C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5956C>A MANE Select ENSP00000298910.7:p.His1986Asn
ENST00000679360.1:c.*4865C>A ENSP00000505368.1:n.*4865C>A
ENST00000679532.1:c.1730C>A
ENST00000680018.1:c.1401C>A ENSP00000505347.1:n.1401C>A
ENST00000680422.1:c.1601C>A
ENST00000680425.1:c.1123C>A ENSP00000506459.1:n.1123C>A
ENST00000680453.1:c.1413C>A
ENST00000680790.1:c.5701C>A ENSP00000505335.1:p.His1901Asn
ENST00000681136.1:n.1940C>A
ENST00000681696.1:c.1639C>A ENSP00000505871.1:p.His547Asn
ENST00000298910.11:c.5956C>A ENSP00000298910.7:p.His1986Asn
ENST00000430804.5:c.3252C>A
ENST00000479187.5:n.2637C>A
NM_198578.3:c.5956C>A NP_940980.3:p.His1986Asn
XM_005268629.2:c.5956C>A XP_005268686.1:p.His1986Asn
XM_011537877.1:c.5956C>A XP_011536179.1:p.His1986Asn
XM_011537878.1:c.5956C>A XP_011536180.1:p.His1986Asn
XM_011537879.1:c.4753C>A XP_011536181.1:p.His1585Asn
XM_005268629.4:c.5956C>A XP_005268686.1:p.His1986Asn
XM_011537877.3:c.5956C>A XP_011536179.1:p.His1986Asn
XM_017018787.1:c.2872C>A XP_016874276.1:p.His958Asn
XM_017018788.2:c.2218C>A XP_016874277.1:p.His740Asn
XM_024448833.1:c.4753C>A XP_024304601.1:p.His1585Asn
NM_198578.4:c.5956C>A MANE Select NP_940980.4:p.His1986Asn