Canonical Allele Identifier: CA343679
Gene: LRRK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39234
dbSNP Id: rs33962975

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363528A>G , CM000674.2:g.40363528A>G GRCh38
NC_000012.11:g.40757330A>G , CM000674.1:g.40757330A>G GRCh37
NC_000012.10:g.39043597A>G NCBI36
NG_011709.1:g.143518A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7155A>G MANE Select ENSP00000298910.7:p.Gly2385=
ENST00000636518.1:c.952A>G
ENST00000679360.1:c.*6064A>G ENSP00000505368.1:n.*6064A>G
ENST00000679532.1:c.2929A>G
ENST00000679683.1:c.945A>G
ENST00000680018.1:c.2600A>G ENSP00000505347.1:n.2600A>G
ENST00000680422.1:c.4242A>G
ENST00000680425.1:c.2322A>G ENSP00000506459.1:n.2322A>G
ENST00000680453.1:c.2612A>G
ENST00000680790.1:c.6900A>G ENSP00000505335.1:p.Gly2300=
ENST00000681136.1:n.3139A>G
ENST00000681696.1:c.2838A>G ENSP00000505871.1:p.Gly946=
ENST00000681773.1:n.362A>G
ENST00000298910.11:c.7155A>G ENSP00000298910.7:p.Gly2385=
ENST00000430804.5:c.4451A>G
ENST00000479187.5:n.3836A>G
NM_198578.3:c.7155A>G NP_940980.3:p.Gly2385=
XM_005268629.2:c.7155A>G XP_005268686.1:p.Gly2385=
XM_011537877.1:c.7155A>G XP_011536179.1:p.Gly2385=
XM_011537879.1:c.5952A>G XP_011536181.1:p.Gly1984=
XR_944868.1:n.485-8701T>C
XM_005268629.4:c.7155A>G XP_005268686.1:p.Gly2385=
XM_011537877.3:c.7155A>G XP_011536179.1:p.Gly2385=
XM_017018787.1:c.4071A>G XP_016874276.1:p.Gly1357=
XM_017018788.2:c.3417A>G XP_016874277.1:p.Gly1139=
XM_024448833.1:c.5952A>G XP_024304601.1:p.Gly1984=
XR_944868.2:n.485-8701T>C
NM_198578.4:c.7155A>G MANE Select NP_940980.4:p.Gly2385=