Canonical Allele Identifier: CA2031001350
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40323257G= , CM000674.2:g.40323257G= GRCh38
NC_000012.11:g.40717059G= , CM000674.1:g.40717059G= GRCh37
NC_000012.10:g.39003326G= NCBI36
NG_011709.1:g.103247G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5607G= MANE Select ENSP00000298910.7:p.Met1869=
ENST00000679360.1:c.*4516G= ENSP00000505368.1:n.*4516G=
ENST00000679532.1:c.1381G=
ENST00000680018.1:c.1052G= ENSP00000505347.1:n.1052G=
ENST00000680422.1:c.1252G=
ENST00000680425.1:c.774G= ENSP00000506459.1:n.774G=
ENST00000680453.1:c.1064G=
ENST00000680790.1:c.5352G= ENSP00000505335.1:p.Met1784=
ENST00000681136.1:n.1591G=
ENST00000681696.1:c.1290G= ENSP00000505871.1:p.Met430=
ENST00000298910.11:c.5607G= ENSP00000298910.7:p.Met1869=
ENST00000430804.5:c.2903G=
ENST00000479187.5:n.2288G=
NM_198578.3:c.5607G= NP_940980.3:p.Met1869=
XM_005268629.2:c.5607G= XP_005268686.1:p.Met1869=
XM_011537877.1:c.5607G= XP_011536179.1:p.Met1869=
XM_011537878.1:c.5607G= XP_011536180.1:p.Met1869=
XM_011537879.1:c.4404G= XP_011536181.1:p.Met1468=
XM_005268629.4:c.5607G= XP_005268686.1:p.Met1869=
XM_011537877.3:c.5607G= XP_011536179.1:p.Met1869=
XM_017018787.1:c.2523G= XP_016874276.1:p.Met841=
XM_017018788.2:c.1869G= XP_016874277.1:p.Met623=
XM_024448833.1:c.4404G= XP_024304601.1:p.Met1468=
NM_198578.4:c.5607G= MANE Select NP_940980.4:p.Met1869=