Canonical Allele Identifier: CA946835241
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs1165516455

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340224A>C , CM000674.2:g.40340224A>C GRCh38
NC_000012.11:g.40734026A>C , CM000674.1:g.40734026A>C GRCh37
NC_000012.10:g.39020293A>C NCBI36
NG_011709.1:g.120214A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5949-70A>C MANE Select ENSP00000298910.7:n.5949-70A>C
ENST00000679360.1:c.*4858-70A>C ENSP00000505368.1:n.*4858-70A>C
ENST00000679532.1:c.1723-70A>C
ENST00000680018.1:c.1394-70A>C ENSP00000505347.1:n.1394-70A>C
ENST00000680422.1:c.1594-70A>C
ENST00000680425.1:c.1116-70A>C ENSP00000506459.1:n.1116-70A>C
ENST00000680453.1:c.1406-70A>C
ENST00000680790.1:c.5694-70A>C ENSP00000505335.1:n.5694-70A>C
ENST00000681136.1:n.1933-70A>C
ENST00000681696.1:c.1632-70A>C ENSP00000505871.1:n.1632-70A>C
ENST00000298910.11:c.5949-70A>C ENSP00000298910.7:n.5949-70A>C
ENST00000430804.5:c.3245-70A>C
ENST00000479187.5:n.2630-70A>C
NM_198578.3:c.5949-70A>C NP_940980.3:n.5949-70A>C
XM_005268629.2:c.5949-70A>C XP_005268686.1:n.5949-70A>C
XM_011537877.1:c.5949-70A>C XP_011536179.1:n.5949-70A>C
XM_011537878.1:c.5949-70A>C XP_011536180.1:n.5949-70A>C
XM_011537879.1:c.4746-70A>C XP_011536181.1:n.4746-70A>C
XM_005268629.4:c.5949-70A>C XP_005268686.1:n.5949-70A>C
XM_011537877.3:c.5949-70A>C XP_011536179.1:n.5949-70A>C
XM_017018787.1:c.2865-70A>C XP_016874276.1:n.2865-70A>C
XM_017018788.2:c.2211-70A>C XP_016874277.1:n.2211-70A>C
XM_024448833.1:c.4746-70A>C XP_024304601.1:n.4746-70A>C
NM_198578.4:c.5949-70A>C MANE Select NP_940980.4:n.5949-70A>C