Canonical Allele Identifier: CA6514601
Gene: LRRK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1751524
ClinVar RCV Id: RCV002360072
dbSNP Id: rs777004444

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340439T>A , CM000674.2:g.40340439T>A GRCh38
NC_000012.11:g.40734241T>A , CM000674.1:g.40734241T>A GRCh37
NC_000012.10:g.39020508T>A NCBI36
NG_011709.1:g.120429T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.6094T>A MANE Select ENSP00000298910.7:p.Ser2032Thr
ENST00000679360.1:c.*5003T>A ENSP00000505368.1:n.*5003T>A
ENST00000679532.1:c.1868T>A
ENST00000680018.1:c.1539T>A ENSP00000505347.1:n.1539T>A
ENST00000680422.1:c.1739T>A
ENST00000680425.1:c.1261T>A ENSP00000506459.1:n.1261T>A
ENST00000680453.1:c.1551T>A
ENST00000680790.1:c.5839T>A ENSP00000505335.1:p.Ser1947Thr
ENST00000681136.1:n.2078T>A
ENST00000681696.1:c.1777T>A ENSP00000505871.1:p.Ser593Thr
ENST00000298910.11:c.6094T>A ENSP00000298910.7:p.Ser2032Thr
ENST00000430804.5:c.3390T>A
ENST00000479187.5:n.2775T>A
NM_198578.3:c.6094T>A NP_940980.3:p.Ser2032Thr
XM_005268629.2:c.6094T>A XP_005268686.1:p.Ser2032Thr
XM_011537877.1:c.6094T>A XP_011536179.1:p.Ser2032Thr
XM_011537878.1:c.6094T>A XP_011536180.1:p.Ser2032Thr
XM_011537879.1:c.4891T>A XP_011536181.1:p.Ser1631Thr
XM_005268629.4:c.6094T>A XP_005268686.1:p.Ser2032Thr
XM_011537877.3:c.6094T>A XP_011536179.1:p.Ser2032Thr
XM_017018787.1:c.3010T>A XP_016874276.1:p.Ser1004Thr
XM_017018788.2:c.2356T>A XP_016874277.1:p.Ser786Thr
XM_024448833.1:c.4891T>A XP_024304601.1:p.Ser1631Thr
NM_198578.4:c.6094T>A MANE Select NP_940980.4:p.Ser2032Thr