Canonical Allele Identifier: CA384413302
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363461T>C , CM000674.2:g.40363461T>C GRCh38
NC_000012.11:g.40757263T>C , CM000674.1:g.40757263T>C GRCh37
NC_000012.10:g.39043530T>C NCBI36
NG_011709.1:g.143451T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.7088T>C MANE Select ENSP00000298910.7:p.Leu2363Pro
ENST00000636518.1:c.885T>C
ENST00000679360.1:c.*5997T>C ENSP00000505368.1:n.*5997T>C
ENST00000679532.1:c.2862T>C
ENST00000679683.1:c.878T>C
ENST00000680018.1:c.2533T>C ENSP00000505347.1:n.2533T>C
ENST00000680422.1:c.4175T>C
ENST00000680425.1:c.2255T>C ENSP00000506459.1:n.2255T>C
ENST00000680453.1:c.2545T>C
ENST00000680790.1:c.6833T>C ENSP00000505335.1:p.Leu2278Pro
ENST00000681136.1:n.3072T>C
ENST00000681696.1:c.2771T>C ENSP00000505871.1:p.Leu924Pro
ENST00000681773.1:n.295T>C
ENST00000298910.11:c.7088T>C ENSP00000298910.7:p.Leu2363Pro
ENST00000430804.5:c.4384T>C
ENST00000479187.5:n.3769T>C
NM_198578.3:c.7088T>C NP_940980.3:p.Leu2363Pro
XM_005268629.2:c.7088T>C XP_005268686.1:p.Leu2363Pro
XM_011537877.1:c.7088T>C XP_011536179.1:p.Leu2363Pro
XM_011537879.1:c.5885T>C XP_011536181.1:p.Leu1962Pro
XR_944868.1:n.485-8634A>G
XM_005268629.4:c.7088T>C XP_005268686.1:p.Leu2363Pro
XM_011537877.3:c.7088T>C XP_011536179.1:p.Leu2363Pro
XM_017018787.1:c.4004T>C XP_016874276.1:p.Leu1335Pro
XM_017018788.2:c.3350T>C XP_016874277.1:p.Leu1117Pro
XM_024448833.1:c.5885T>C XP_024304601.1:p.Leu1962Pro
XR_944868.2:n.485-8634A>G
NM_198578.4:c.7088T>C MANE Select NP_940980.4:p.Leu2363Pro