Canonical Allele Identifier: CA384413161
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363426T>G , CM000674.2:g.40363426T>G GRCh38
NC_000012.11:g.40757228T>G , CM000674.1:g.40757228T>G GRCh37
NC_000012.10:g.39043495T>G NCBI36
NG_011709.1:g.143416T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7053T>G MANE Select ENSP00000298910.7:p.Asp2351Glu
ENST00000636518.1:c.850T>G
ENST00000679360.1:c.*5962T>G ENSP00000505368.1:n.*5962T>G
ENST00000679532.1:c.2827T>G
ENST00000679683.1:c.843T>G
ENST00000680018.1:c.2498T>G ENSP00000505347.1:n.2498T>G
ENST00000680422.1:c.4140T>G
ENST00000680425.1:c.2220T>G ENSP00000506459.1:n.2220T>G
ENST00000680453.1:c.2510T>G
ENST00000680790.1:c.6798T>G ENSP00000505335.1:p.Asp2266Glu
ENST00000681136.1:n.3037T>G
ENST00000681696.1:c.2736T>G ENSP00000505871.1:p.Asp912Glu
ENST00000681773.1:n.260T>G
ENST00000298910.11:c.7053T>G ENSP00000298910.7:p.Asp2351Glu
ENST00000430804.5:c.4349T>G
ENST00000479187.5:n.3734T>G
NM_198578.3:c.7053T>G NP_940980.3:p.Asp2351Glu
XM_005268629.2:c.7053T>G XP_005268686.1:p.Asp2351Glu
XM_011537877.1:c.7053T>G XP_011536179.1:p.Asp2351Glu
XM_011537879.1:c.5850T>G XP_011536181.1:p.Asp1950Glu
XR_944868.1:n.485-8599A>C
XM_005268629.4:c.7053T>G XP_005268686.1:p.Asp2351Glu
XM_011537877.3:c.7053T>G XP_011536179.1:p.Asp2351Glu
XM_017018787.1:c.3969T>G XP_016874276.1:p.Asp1323Glu
XM_017018788.2:c.3315T>G XP_016874277.1:p.Asp1105Glu
XM_024448833.1:c.5850T>G XP_024304601.1:p.Asp1950Glu
XR_944868.2:n.485-8599A>C
NM_198578.4:c.7053T>G MANE Select NP_940980.4:p.Asp2351Glu