Canonical Allele Identifier: CA604504349
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs1213697565

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40323073T>C , CM000674.2:g.40323073T>C GRCh38
NC_000012.11:g.40716875T>C , CM000674.1:g.40716875T>C GRCh37
NC_000012.10:g.39003142T>C NCBI36
NG_011709.1:g.103063T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5510-87T>C MANE Select ENSP00000298910.7:n.5510-87T>C
ENST00000679360.1:c.*4419-87T>C ENSP00000505368.1:n.*4419-87T>C
ENST00000679532.1:c.1284-87T>C
ENST00000680018.1:c.955-87T>C ENSP00000505347.1:n.955-87T>C
ENST00000680422.1:c.1155-87T>C
ENST00000680425.1:c.677-87T>C ENSP00000506459.1:n.677-87T>C
ENST00000680453.1:c.967-87T>C
ENST00000680790.1:c.5255-87T>C ENSP00000505335.1:n.5255-87T>C
ENST00000681136.1:n.1494-87T>C
ENST00000681696.1:c.1193-87T>C ENSP00000505871.1:n.1193-87T>C
ENST00000298910.11:c.5510-87T>C ENSP00000298910.7:n.5510-87T>C
ENST00000430804.5:c.2806-87T>C
ENST00000479187.5:n.2191-87T>C
NM_198578.3:c.5510-87T>C NP_940980.3:n.5510-87T>C
XM_005268629.2:c.5510-87T>C XP_005268686.1:n.5510-87T>C
XM_011537877.1:c.5510-87T>C XP_011536179.1:n.5510-87T>C
XM_011537878.1:c.5510-87T>C XP_011536180.1:n.5510-87T>C
XM_011537879.1:c.4307-87T>C XP_011536181.1:n.4307-87T>C
XM_005268629.4:c.5510-87T>C XP_005268686.1:n.5510-87T>C
XM_011537877.3:c.5510-87T>C XP_011536179.1:n.5510-87T>C
XM_017018787.1:c.2426-87T>C XP_016874276.1:n.2426-87T>C
XM_017018788.2:c.1772-87T>C XP_016874277.1:n.1772-87T>C
XM_024448833.1:c.4307-87T>C XP_024304601.1:n.4307-87T>C
NM_198578.4:c.5510-87T>C MANE Select NP_940980.4:n.5510-87T>C