Canonical Allele Identifier: CA339920
Gene: LRRK2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 1937
ClinVar RCV Id: RCV000002014
dbSNP Id: rs35801418

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40321114A>G , CM000674.2:g.40321114A>G GRCh38
NC_000012.10:g.39001183A>G NCBI36
NC_000012.11:g.40714916A>G , CM000674.1:g.40714916A>G GRCh37
NG_011709.1:g.101104A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.11:c.5096A>G ENSP00000298910.7:p.Tyr1699Cys
ENST00000430804.5:n.2392A>G
ENST00000479187.5:n.1777A>G
NM_198578.3:c.5096A>G VV NP_940980.3:p.Tyr1699Cys
XM_005268629.2:c.5096A>G XP_005268686.1:p.Tyr1699Cys
XM_011537877.1:c.5096A>G XP_011536179.1:p.Tyr1699Cys
XM_011537878.1:c.5096A>G XP_011536180.1:p.Tyr1699Cys
XM_011537879.1:c.3893A>G XP_011536181.1:p.Tyr1298Cys
XM_011537881.1:c.*72A>G XP_011536183.1:p.=
XM_005268629.4:c.5096A>G
XM_011537877.3:c.5096A>G
XM_011537881.3:c.*72A>G
XM_017018787.1:c.2012A>G XP_016874276.1:p.Tyr671Cys
XM_017018788.2:c.1358A>G XP_016874277.1:p.Tyr453Cys
XM_024448833.1:c.3893A>G XP_024304601.1:p.Tyr1298Cys
XR_001748574.2:n.5464A>G