Canonical Allele Identifier: CA2031002676
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40309124G= , CM000674.2:g.40309124G= GRCh38
NC_000012.11:g.40702926G= , CM000674.1:g.40702926G= GRCh37
NC_000012.10:g.38989193G= NCBI36
NG_011709.1:g.89114G=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.4208G= MANE Select ENSP00000298910.7:p.Ser1403=
ENST00000679360.1:c.*3117G= ENSP00000505368.1:n.*3117G=
ENST00000680790.1:c.3953G= ENSP00000505335.1:p.Ser1318=
ENST00000298910.11:c.4208G= ENSP00000298910.7:p.Ser1403=
ENST00000430804.5:c.1504G=
ENST00000479187.5:n.889G=
NM_198578.3:c.4208G= NP_940980.3:p.Ser1403=
XM_005268629.2:c.4208G= XP_005268686.1:p.Ser1403=
XM_011537877.1:c.4208G= XP_011536179.1:p.Ser1403=
XM_011537878.1:c.4208G= XP_011536180.1:p.Ser1403=
XM_011537879.1:c.3005G= XP_011536181.1:p.Ser1002=
XM_011537880.1:c.4208G= XP_011536182.1:p.Ser1403=
XM_011537881.1:c.4208G= XP_011536183.1:p.Ser1403=
XM_005268629.4:c.4208G= XP_005268686.1:p.Ser1403=
XM_011537877.3:c.4208G= XP_011536179.1:p.Ser1403=
XM_011537881.3:c.4208G= XP_011536183.1:p.Ser1403=
XM_017018786.2:c.4208G= XP_016874275.1:p.Ser1403=
XM_017018787.1:c.1124G= XP_016874276.1:p.Ser375=
XM_017018788.2:c.470G= XP_016874277.1:p.Ser157=
XM_024448833.1:c.3005G= XP_024304601.1:p.Ser1002=
XR_001748574.2:n.4450G=
NM_198578.4:c.4208G= MANE Select NP_940980.4:p.Ser1403=