Canonical Allele Identifier: CA384419787
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40320174A>G , CM000674.2:g.40320174A>G GRCh38
NC_000012.11:g.40713976A>G , CM000674.1:g.40713976A>G GRCh37
NC_000012.10:g.39000243A>G NCBI36
NG_011709.1:g.100164A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5014A>G MANE Select ENSP00000298910.7:p.Ser1672Gly
ENST00000679360.1:c.*3923A>G ENSP00000505368.1:n.*3923A>G
ENST00000679532.1:c.788A>G
ENST00000680018.1:c.459A>G ENSP00000505347.1:n.459A>G
ENST00000680422.1:c.659A>G
ENST00000680425.1:c.183-860A>G ENSP00000506459.1:n.183-860A>G
ENST00000680453.1:c.473-860A>G
ENST00000680790.1:c.4759A>G ENSP00000505335.1:p.Ser1587Gly
ENST00000681136.1:n.998A>G
ENST00000681696.1:c.697A>G ENSP00000505871.1:p.Ser233Gly
ENST00000298910.11:c.5014A>G ENSP00000298910.7:p.Ser1672Gly
ENST00000430804.5:c.2310A>G
ENST00000479187.5:n.1695A>G
NM_198578.3:c.5014A>G NP_940980.3:p.Ser1672Gly
XM_005268629.2:c.5014A>G XP_005268686.1:p.Ser1672Gly
XM_011537877.1:c.5014A>G XP_011536179.1:p.Ser1672Gly
XM_011537878.1:c.5014A>G XP_011536180.1:p.Ser1672Gly
XM_011537879.1:c.3811A>G XP_011536181.1:p.Ser1271Gly
XM_011537881.1:c.4828-860A>G XP_011536183.1:n.4828-860A>G
XM_005268629.4:c.5014A>G XP_005268686.1:p.Ser1672Gly
XM_011537877.3:c.5014A>G XP_011536179.1:p.Ser1672Gly
XM_011537881.3:c.4828-860A>G XP_011536183.1:n.4828-860A>G
XM_017018787.1:c.1930A>G XP_016874276.1:p.Ser644Gly
XM_017018788.2:c.1276A>G XP_016874277.1:p.Ser426Gly
XM_024448833.1:c.3811A>G XP_024304601.1:p.Ser1271Gly
XR_001748574.2:n.5382A>G
NM_198578.4:c.5014A>G MANE Select NP_940980.4:p.Ser1672Gly