Canonical Allele Identifier: CA384415724
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40299179C>A , CM000674.2:g.40299179C>A GRCh38
NC_000012.11:g.40692981C>A , CM000674.1:g.40692981C>A GRCh37
NC_000012.10:g.38979248C>A NCBI36
NG_011709.1:g.79169C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3418C>A MANE Select ENSP00000298910.7:p.His1140Asn
ENST00000679360.1:c.*2327C>A ENSP00000505368.1:n.*2327C>A
ENST00000680790.1:c.3163C>A ENSP00000505335.1:p.His1055Asn
ENST00000298910.11:c.3418C>A ENSP00000298910.7:p.His1140Asn
ENST00000343742.6:c.3418C>A ENSP00000341930.2:p.His1140Asn
ENST00000430804.5:c.462C>A
ENST00000479187.5:n.99C>A
NM_198578.3:c.3418C>A NP_940980.3:p.His1140Asn
XM_005268629.2:c.3418C>A XP_005268686.1:p.His1140Asn
XM_011537877.1:c.3418C>A XP_011536179.1:p.His1140Asn
XM_011537878.1:c.3418C>A XP_011536180.1:p.His1140Asn
XM_011537879.1:c.2215C>A XP_011536181.1:p.His739Asn
XM_011537880.1:c.3418C>A XP_011536182.1:p.His1140Asn
XM_011537881.1:c.3418C>A XP_011536183.1:p.His1140Asn
XM_011537882.1:c.3418C>A XP_011536184.1:p.His1140Asn
XM_005268629.4:c.3418C>A XP_005268686.1:p.His1140Asn
XM_011537877.3:c.3418C>A XP_011536179.1:p.His1140Asn
XM_011537881.3:c.3418C>A XP_011536183.1:p.His1140Asn
XM_011537882.3:c.3418C>A XP_011536184.1:p.His1140Asn
XM_017018786.2:c.3418C>A XP_016874275.1:p.His1140Asn
XM_017018787.1:c.334C>A XP_016874276.1:p.His112Asn
XM_017018789.2:c.3418C>A XP_016874278.1:p.His1140Asn
XM_024448833.1:c.2215C>A XP_024304601.1:p.His739Asn
XR_001748574.2:n.3660C>A
NM_198578.4:c.3418C>A MANE Select NP_940980.4:p.His1140Asn