Canonical Allele Identifier: CA384419789
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40320175G>A , CM000674.2:g.40320175G>A GRCh38
NC_000012.11:g.40713977G>A , CM000674.1:g.40713977G>A GRCh37
NC_000012.10:g.39000244G>A NCBI36
NG_011709.1:g.100165G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5015G>A MANE Select ENSP00000298910.7:p.Ser1672Asn
ENST00000679360.1:c.*3924G>A ENSP00000505368.1:n.*3924G>A
ENST00000679532.1:c.789G>A
ENST00000680018.1:c.460G>A ENSP00000505347.1:n.460G>A
ENST00000680422.1:c.660G>A
ENST00000680425.1:c.183-859G>A ENSP00000506459.1:n.183-859G>A
ENST00000680453.1:c.473-859G>A
ENST00000680790.1:c.4760G>A ENSP00000505335.1:p.Ser1587Asn
ENST00000681136.1:n.999G>A
ENST00000681696.1:c.698G>A ENSP00000505871.1:p.Ser233Asn
ENST00000298910.11:c.5015G>A ENSP00000298910.7:p.Ser1672Asn
ENST00000430804.5:c.2311G>A
ENST00000479187.5:n.1696G>A
NM_198578.3:c.5015G>A NP_940980.3:p.Ser1672Asn
XM_005268629.2:c.5015G>A XP_005268686.1:p.Ser1672Asn
XM_011537877.1:c.5015G>A XP_011536179.1:p.Ser1672Asn
XM_011537878.1:c.5015G>A XP_011536180.1:p.Ser1672Asn
XM_011537879.1:c.3812G>A XP_011536181.1:p.Ser1271Asn
XM_011537881.1:c.4828-859G>A XP_011536183.1:n.4828-859G>A
XM_005268629.4:c.5015G>A XP_005268686.1:p.Ser1672Asn
XM_011537877.3:c.5015G>A XP_011536179.1:p.Ser1672Asn
XM_011537881.3:c.4828-859G>A XP_011536183.1:n.4828-859G>A
XM_017018787.1:c.1931G>A XP_016874276.1:p.Ser644Asn
XM_017018788.2:c.1277G>A XP_016874277.1:p.Ser426Asn
XM_024448833.1:c.3812G>A XP_024304601.1:p.Ser1271Asn
XR_001748574.2:n.5383G>A
NM_198578.4:c.5015G>A MANE Select NP_940980.4:p.Ser1672Asn