Canonical Allele Identifier: CA2031025806
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363439A= , CM000674.2:g.40363439A= GRCh38
NC_000012.11:g.40757241A= , CM000674.1:g.40757241A= GRCh37
NC_000012.10:g.39043508A= NCBI36
NG_011709.1:g.143429A=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7066A= MANE Select ENSP00000298910.7:p.Thr2356=
ENST00000636518.1:c.863A=
ENST00000679360.1:c.*5975A= ENSP00000505368.1:n.*5975A=
ENST00000679532.1:c.2840A=
ENST00000679683.1:c.856A=
ENST00000680018.1:c.2511A= ENSP00000505347.1:n.2511A=
ENST00000680422.1:c.4153A=
ENST00000680425.1:c.2233A= ENSP00000506459.1:n.2233A=
ENST00000680453.1:c.2523A=
ENST00000680790.1:c.6811A= ENSP00000505335.1:p.Thr2271=
ENST00000681136.1:n.3050A=
ENST00000681696.1:c.2749A= ENSP00000505871.1:p.Thr917=
ENST00000681773.1:n.273A=
ENST00000298910.11:c.7066A= ENSP00000298910.7:p.Thr2356=
ENST00000430804.5:c.4362A=
ENST00000479187.5:n.3747A=
NM_198578.3:c.7066A= NP_940980.3:p.Thr2356=
XM_005268629.2:c.7066A= XP_005268686.1:p.Thr2356=
XM_011537877.1:c.7066A= XP_011536179.1:p.Thr2356=
XM_011537879.1:c.5863A= XP_011536181.1:p.Thr1955=
XR_944868.1:n.485-8612T=
XM_005268629.4:c.7066A= XP_005268686.1:p.Thr2356=
XM_011537877.3:c.7066A= XP_011536179.1:p.Thr2356=
XM_017018787.1:c.3982A= XP_016874276.1:p.Thr1328=
XM_017018788.2:c.3328A= XP_016874277.1:p.Thr1110=
XM_024448833.1:c.5863A= XP_024304601.1:p.Thr1955=
XR_944868.2:n.485-8612T=
NM_198578.4:c.7066A= MANE Select NP_940980.4:p.Thr2356=