Canonical Allele Identifier: CA2030982823
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298403A= , CM000674.2:g.40298403A= GRCh38
NC_000012.11:g.40692205A= , CM000674.1:g.40692205A= GRCh37
NC_000012.10:g.38978472A= NCBI36
NG_011709.1:g.78393A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3257A= MANE Select ENSP00000298910.7:p.Lys1086=
ENST00000679360.1:c.*2166A= ENSP00000505368.1:n.*2166A=
ENST00000680790.1:c.3002A= ENSP00000505335.1:p.Lys1001=
ENST00000298910.11:c.3257A= ENSP00000298910.7:p.Lys1086=
ENST00000343742.6:c.3257A= ENSP00000341930.2:p.Lys1086=
ENST00000430804.5:c.301A=
NM_198578.3:c.3257A= NP_940980.3:p.Lys1086=
XM_005268629.2:c.3257A= XP_005268686.1:p.Lys1086=
XM_011537877.1:c.3257A= XP_011536179.1:p.Lys1086=
XM_011537878.1:c.3257A= XP_011536180.1:p.Lys1086=
XM_011537879.1:c.2054A= XP_011536181.1:p.Lys685=
XM_011537880.1:c.3257A= XP_011536182.1:p.Lys1086=
XM_011537881.1:c.3257A= XP_011536183.1:p.Lys1086=
XM_011537882.1:c.3257A= XP_011536184.1:p.Lys1086=
XM_005268629.4:c.3257A= XP_005268686.1:p.Lys1086=
XM_011537877.3:c.3257A= XP_011536179.1:p.Lys1086=
XM_011537881.3:c.3257A= XP_011536183.1:p.Lys1086=
XM_011537882.3:c.3257A= XP_011536184.1:p.Lys1086=
XM_017018786.2:c.3257A= XP_016874275.1:p.Lys1086=
XM_017018787.1:c.173A= XP_016874276.1:p.Lys58=
XM_017018789.2:c.3257A= XP_016874278.1:p.Lys1086=
XM_024448833.1:c.2054A= XP_024304601.1:p.Lys685=
XR_001748574.2:n.3499A=
NM_198578.4:c.3257A= MANE Select NP_940980.4:p.Lys1086=