Canonical Allele Identifier: CA2031027031
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs1592311148

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340241A>G , CM000674.2:g.40340241A>G GRCh38
NC_000012.11:g.40734043A>G , CM000674.1:g.40734043A>G GRCh37
NC_000012.10:g.39020310A>G NCBI36
NG_011709.1:g.120231A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5949-53A>G MANE Select ENSP00000298910.7:n.5949-53A>G
ENST00000679360.1:c.*4858-53A>G ENSP00000505368.1:n.*4858-53A>G
ENST00000679532.1:c.1723-53A>G
ENST00000680018.1:c.1394-53A>G ENSP00000505347.1:n.1394-53A>G
ENST00000680422.1:c.1594-53A>G
ENST00000680425.1:c.1116-53A>G ENSP00000506459.1:n.1116-53A>G
ENST00000680453.1:c.1406-53A>G
ENST00000680790.1:c.5694-53A>G ENSP00000505335.1:n.5694-53A>G
ENST00000681136.1:n.1933-53A>G
ENST00000681696.1:c.1632-53A>G ENSP00000505871.1:n.1632-53A>G
ENST00000298910.11:c.5949-53A>G ENSP00000298910.7:n.5949-53A>G
ENST00000430804.5:c.3245-53A>G
ENST00000479187.5:n.2630-53A>G
NM_198578.3:c.5949-53A>G NP_940980.3:n.5949-53A>G
XM_005268629.2:c.5949-53A>G XP_005268686.1:n.5949-53A>G
XM_011537877.1:c.5949-53A>G XP_011536179.1:n.5949-53A>G
XM_011537878.1:c.5949-53A>G XP_011536180.1:n.5949-53A>G
XM_011537879.1:c.4746-53A>G XP_011536181.1:n.4746-53A>G
XM_005268629.4:c.5949-53A>G XP_005268686.1:n.5949-53A>G
XM_011537877.3:c.5949-53A>G XP_011536179.1:n.5949-53A>G
XM_017018787.1:c.2865-53A>G XP_016874276.1:n.2865-53A>G
XM_017018788.2:c.2211-53A>G XP_016874277.1:n.2211-53A>G
XM_024448833.1:c.4746-53A>G XP_024304601.1:n.4746-53A>G
NM_198578.4:c.5949-53A>G MANE Select NP_940980.4:n.5949-53A>G