Canonical Allele Identifier: CA384404003
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340407C>T , CM000674.2:g.40340407C>T GRCh38
NC_000012.11:g.40734209C>T , CM000674.1:g.40734209C>T GRCh37
NC_000012.10:g.39020476C>T NCBI36
NG_011709.1:g.120397C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.6062C>T MANE Select ENSP00000298910.7:p.Ala2021Val
ENST00000679360.1:c.*4971C>T ENSP00000505368.1:n.*4971C>T
ENST00000679532.1:c.1836C>T
ENST00000680018.1:c.1507C>T ENSP00000505347.1:n.1507C>T
ENST00000680422.1:c.1707C>T
ENST00000680425.1:c.1229C>T ENSP00000506459.1:n.1229C>T
ENST00000680453.1:c.1519C>T
ENST00000680790.1:c.5807C>T ENSP00000505335.1:p.Ala1936Val
ENST00000681136.1:n.2046C>T
ENST00000681696.1:c.1745C>T ENSP00000505871.1:p.Ala582Val
ENST00000298910.11:c.6062C>T ENSP00000298910.7:p.Ala2021Val
ENST00000430804.5:c.3358C>T
ENST00000479187.5:n.2743C>T
NM_198578.3:c.6062C>T NP_940980.3:p.Ala2021Val
XM_005268629.2:c.6062C>T XP_005268686.1:p.Ala2021Val
XM_011537877.1:c.6062C>T XP_011536179.1:p.Ala2021Val
XM_011537878.1:c.6062C>T XP_011536180.1:p.Ala2021Val
XM_011537879.1:c.4859C>T XP_011536181.1:p.Ala1620Val
XM_005268629.4:c.6062C>T XP_005268686.1:p.Ala2021Val
XM_011537877.3:c.6062C>T XP_011536179.1:p.Ala2021Val
XM_017018787.1:c.2978C>T XP_016874276.1:p.Ala993Val
XM_017018788.2:c.2324C>T XP_016874277.1:p.Ala775Val
XM_024448833.1:c.4859C>T XP_024304601.1:p.Ala1620Val
NM_198578.4:c.6062C>T MANE Select NP_940980.4:p.Ala2021Val