Canonical Allele Identifier: CA2030996773
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40321014T= , CM000674.2:g.40321014T= GRCh38
NC_000012.11:g.40714816T= , CM000674.1:g.40714816T= GRCh37
NC_000012.10:g.39001083T= NCBI36
NG_011709.1:g.101004T=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5016-20T= MANE Select ENSP00000298910.7:n.5016-20T=
ENST00000679360.1:c.*3925-20T= ENSP00000505368.1:n.*3925-20T=
ENST00000679532.1:c.790-20T=
ENST00000680018.1:c.461-20T= ENSP00000505347.1:n.461-20T=
ENST00000680422.1:c.661-20T=
ENST00000680425.1:c.183-20T= ENSP00000506459.1:n.183-20T=
ENST00000680453.1:c.473-20T=
ENST00000680790.1:c.4761-20T= ENSP00000505335.1:n.4761-20T=
ENST00000681136.1:n.1000-20T=
ENST00000681696.1:c.699-20T= ENSP00000505871.1:n.699-20T=
ENST00000298910.11:c.5016-20T= ENSP00000298910.7:n.5016-20T=
ENST00000430804.5:c.2312-20T=
ENST00000479187.5:n.1697-20T=
NM_198578.3:c.5016-20T= NP_940980.3:n.5016-20T=
XM_005268629.2:c.5016-20T= XP_005268686.1:n.5016-20T=
XM_011537877.1:c.5016-20T= XP_011536179.1:n.5016-20T=
XM_011537878.1:c.5016-20T= XP_011536180.1:n.5016-20T=
XM_011537879.1:c.3813-20T= XP_011536181.1:n.3813-20T=
XM_011537881.1:c.4828-20T= XP_011536183.1:n.4828-20T=
XM_005268629.4:c.5016-20T= XP_005268686.1:n.5016-20T=
XM_011537877.3:c.5016-20T= XP_011536179.1:n.5016-20T=
XM_011537881.3:c.4828-20T= XP_011536183.1:n.4828-20T=
XM_017018787.1:c.1932-20T= XP_016874276.1:n.1932-20T=
XM_017018788.2:c.1278-20T= XP_016874277.1:n.1278-20T=
XM_024448833.1:c.3813-20T= XP_024304601.1:n.3813-20T=
XR_001748574.2:n.5384-20T=
NM_198578.4:c.5016-20T= MANE Select NP_940980.4:n.5016-20T=