Canonical Allele Identifier: CA10641166
Gene: LRRK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 308650
dbSNP Id: rs66737902

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40367861T>C , CM000674.2:g.40367861T>C GRCh38
NC_000012.11:g.40761663T>C , CM000674.1:g.40761663T>C GRCh37
NC_000012.10:g.39047930T>C NCBI36
NG_011709.1:g.147851T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.*96T>C MANE Select ENSP00000298910.7:n.*96T>C
ENST00000636518.1:c.1459T>C
ENST00000679532.1:c.3454T>C
ENST00000679683.1:c.1470T>C
ENST00000680018.1:c.3125T>C ENSP00000505347.1:n.3125T>C
ENST00000680422.1:c.7288T>C
ENST00000680425.1:c.2775T>C ENSP00000506459.1:n.2775T>C
ENST00000680453.1:c.3119T>C
ENST00000680790.1:c.*96T>C ENSP00000505335.1:n.*96T>C
ENST00000681136.1:n.3612T>C
ENST00000681696.1:c.3359T>C ENSP00000505871.1:n.3359T>C
ENST00000681773.1:n.3408T>C
ENST00000298910.11:c.*96T>C ENSP00000298910.7:n.*96T>C
ENST00000430804.5:c.4976T>C
ENST00000479187.5:n.6882T>C
NM_198578.3:c.*96T>C NP_940980.3:n.*96T>C
XM_005268629.2:c.*96T>C XP_005268686.1:n.*96T>C
XM_011537877.1:c.*96T>C XP_011536179.1:n.*96T>C
XM_011537879.1:c.*96T>C XP_011536181.1:n.*96T>C
XR_944868.1:n.485-13034A>G
XM_005268629.4:c.*96T>C XP_005268686.1:n.*96T>C
XM_011537877.3:c.*96T>C XP_011536179.1:n.*96T>C
XM_017018787.1:c.*96T>C XP_016874276.1:n.*96T>C
XM_017018788.2:c.*96T>C XP_016874277.1:n.*96T>C
XM_024448833.1:c.*96T>C XP_024304601.1:n.*96T>C
XR_944868.2:n.485-13034A>G
NM_198578.4:c.*96T>C MANE Select NP_940980.4:n.*96T>C