Canonical Allele Identifier: CA384403856
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340373G>T , CM000674.2:g.40340373G>T GRCh38
NC_000012.11:g.40734175G>T , CM000674.1:g.40734175G>T GRCh37
NC_000012.10:g.39020442G>T NCBI36
NG_011709.1:g.120363G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.6028G>T MANE Select ENSP00000298910.7:p.Ala2010Ser
ENST00000679360.1:c.*4937G>T ENSP00000505368.1:n.*4937G>T
ENST00000679532.1:c.1802G>T
ENST00000680018.1:c.1473G>T ENSP00000505347.1:n.1473G>T
ENST00000680422.1:c.1673G>T
ENST00000680425.1:c.1195G>T ENSP00000506459.1:n.1195G>T
ENST00000680453.1:c.1485G>T
ENST00000680790.1:c.5773G>T ENSP00000505335.1:p.Ala1925Ser
ENST00000681136.1:n.2012G>T
ENST00000681696.1:c.1711G>T ENSP00000505871.1:p.Ala571Ser
ENST00000298910.11:c.6028G>T ENSP00000298910.7:p.Ala2010Ser
ENST00000430804.5:c.3324G>T
ENST00000479187.5:n.2709G>T
NM_198578.3:c.6028G>T NP_940980.3:p.Ala2010Ser
XM_005268629.2:c.6028G>T XP_005268686.1:p.Ala2010Ser
XM_011537877.1:c.6028G>T XP_011536179.1:p.Ala2010Ser
XM_011537878.1:c.6028G>T XP_011536180.1:p.Ala2010Ser
XM_011537879.1:c.4825G>T XP_011536181.1:p.Ala1609Ser
XM_005268629.4:c.6028G>T XP_005268686.1:p.Ala2010Ser
XM_011537877.3:c.6028G>T XP_011536179.1:p.Ala2010Ser
XM_017018787.1:c.2944G>T XP_016874276.1:p.Ala982Ser
XM_017018788.2:c.2290G>T XP_016874277.1:p.Ala764Ser
XM_024448833.1:c.4825G>T XP_024304601.1:p.Ala1609Ser
NM_198578.4:c.6028G>T MANE Select NP_940980.4:p.Ala2010Ser