Canonical Allele Identifier: CA2030982851
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298472T= , CM000674.2:g.40298472T= GRCh38
NC_000012.11:g.40692274T= , CM000674.1:g.40692274T= GRCh37
NC_000012.10:g.38978541T= NCBI36
NG_011709.1:g.78462T=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.3326T= MANE Select ENSP00000298910.7:p.Leu1109=
ENST00000679360.1:c.*2235T= ENSP00000505368.1:n.*2235T=
ENST00000680790.1:c.3071T= ENSP00000505335.1:p.Leu1024=
ENST00000298910.11:c.3326T= ENSP00000298910.7:p.Leu1109=
ENST00000343742.6:c.3326T= ENSP00000341930.2:p.Leu1109=
ENST00000430804.5:c.370T=
ENST00000479187.5:n.7T=
NM_198578.3:c.3326T= NP_940980.3:p.Leu1109=
XM_005268629.2:c.3326T= XP_005268686.1:p.Leu1109=
XM_011537877.1:c.3326T= XP_011536179.1:p.Leu1109=
XM_011537878.1:c.3326T= XP_011536180.1:p.Leu1109=
XM_011537879.1:c.2123T= XP_011536181.1:p.Leu708=
XM_011537880.1:c.3326T= XP_011536182.1:p.Leu1109=
XM_011537881.1:c.3326T= XP_011536183.1:p.Leu1109=
XM_011537882.1:c.3326T= XP_011536184.1:p.Leu1109=
XM_005268629.4:c.3326T= XP_005268686.1:p.Leu1109=
XM_011537877.3:c.3326T= XP_011536179.1:p.Leu1109=
XM_011537881.3:c.3326T= XP_011536183.1:p.Leu1109=
XM_011537882.3:c.3326T= XP_011536184.1:p.Leu1109=
XM_017018786.2:c.3326T= XP_016874275.1:p.Leu1109=
XM_017018787.1:c.242T= XP_016874276.1:p.Leu81=
XM_017018789.2:c.3326T= XP_016874278.1:p.Leu1109=
XM_024448833.1:c.2123T= XP_024304601.1:p.Leu708=
XR_001748574.2:n.3568T=
NM_198578.4:c.3326T= MANE Select NP_940980.4:p.Leu1109=