Canonical Allele Identifier: CA2031025799
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363438A= , CM000674.2:g.40363438A= GRCh38
NC_000012.11:g.40757240A= , CM000674.1:g.40757240A= GRCh37
NC_000012.10:g.39043507A= NCBI36
NG_011709.1:g.143428A=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7065A= MANE Select ENSP00000298910.7:p.Ile2355=
ENST00000636518.1:c.862A=
ENST00000679360.1:c.*5974A= ENSP00000505368.1:n.*5974A=
ENST00000679532.1:c.2839A=
ENST00000679683.1:c.855A=
ENST00000680018.1:c.2510A= ENSP00000505347.1:n.2510A=
ENST00000680422.1:c.4152A=
ENST00000680425.1:c.2232A= ENSP00000506459.1:n.2232A=
ENST00000680453.1:c.2522A=
ENST00000680790.1:c.6810A= ENSP00000505335.1:p.Ile2270=
ENST00000681136.1:n.3049A=
ENST00000681696.1:c.2748A= ENSP00000505871.1:p.Ile916=
ENST00000681773.1:n.272A=
ENST00000298910.11:c.7065A= ENSP00000298910.7:p.Ile2355=
ENST00000430804.5:c.4361A=
ENST00000479187.5:n.3746A=
NM_198578.3:c.7065A= NP_940980.3:p.Ile2355=
XM_005268629.2:c.7065A= XP_005268686.1:p.Ile2355=
XM_011537877.1:c.7065A= XP_011536179.1:p.Ile2355=
XM_011537879.1:c.5862A= XP_011536181.1:p.Ile1954=
XR_944868.1:n.485-8611T=
XM_005268629.4:c.7065A= XP_005268686.1:p.Ile2355=
XM_011537877.3:c.7065A= XP_011536179.1:p.Ile2355=
XM_017018787.1:c.3981A= XP_016874276.1:p.Ile1327=
XM_017018788.2:c.3327A= XP_016874277.1:p.Ile1109=
XM_024448833.1:c.5862A= XP_024304601.1:p.Ile1954=
XR_944868.2:n.485-8611T=
NM_198578.4:c.7065A= MANE Select NP_940980.4:p.Ile2355=