Canonical Allele Identifier: CA2031001048
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40323073T= , CM000674.2:g.40323073T= GRCh38
NC_000012.11:g.40716875T= , CM000674.1:g.40716875T= GRCh37
NC_000012.10:g.39003142T= NCBI36
NG_011709.1:g.103063T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5510-87T= MANE Select ENSP00000298910.7:n.5510-87T=
ENST00000679360.1:c.*4419-87T= ENSP00000505368.1:n.*4419-87T=
ENST00000679532.1:c.1284-87T=
ENST00000680018.1:c.955-87T= ENSP00000505347.1:n.955-87T=
ENST00000680422.1:c.1155-87T=
ENST00000680425.1:c.677-87T= ENSP00000506459.1:n.677-87T=
ENST00000680453.1:c.967-87T=
ENST00000680790.1:c.5255-87T= ENSP00000505335.1:n.5255-87T=
ENST00000681136.1:n.1494-87T=
ENST00000681696.1:c.1193-87T= ENSP00000505871.1:n.1193-87T=
ENST00000298910.11:c.5510-87T= ENSP00000298910.7:n.5510-87T=
ENST00000430804.5:c.2806-87T=
ENST00000479187.5:n.2191-87T=
NM_198578.3:c.5510-87T= NP_940980.3:n.5510-87T=
XM_005268629.2:c.5510-87T= XP_005268686.1:n.5510-87T=
XM_011537877.1:c.5510-87T= XP_011536179.1:n.5510-87T=
XM_011537878.1:c.5510-87T= XP_011536180.1:n.5510-87T=
XM_011537879.1:c.4307-87T= XP_011536181.1:n.4307-87T=
XM_005268629.4:c.5510-87T= XP_005268686.1:n.5510-87T=
XM_011537877.3:c.5510-87T= XP_011536179.1:n.5510-87T=
XM_017018787.1:c.2426-87T= XP_016874276.1:n.2426-87T=
XM_017018788.2:c.1772-87T= XP_016874277.1:n.1772-87T=
XM_024448833.1:c.4307-87T= XP_024304601.1:n.4307-87T=
NM_198578.4:c.5510-87T= MANE Select NP_940980.4:n.5510-87T=