Canonical Allele Identifier: CA2030915931
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40263824C= , CM000674.2:g.40263824C= GRCh38
NC_000012.11:g.40657626C= , CM000674.1:g.40657626C= GRCh37
NC_000012.10:g.38943893C= NCBI36
NG_011709.1:g.43814C=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.1579C= MANE Select ENSP00000298910.7:p.His527=
ENST00000679360.1:c.*488C= ENSP00000505368.1:n.*488C=
ENST00000680790.1:c.1324C= ENSP00000505335.1:p.His442=
ENST00000298910.11:c.1579C= ENSP00000298910.7:p.His527=
ENST00000343742.6:c.1579C= ENSP00000341930.2:p.His527=
ENST00000416796.5:c.823C= ENSP00000398726.1:p.His275=
NM_198578.3:c.1579C= NP_940980.3:p.His527=
XM_005268629.2:c.1579C= XP_005268686.1:p.His527=
XM_011537877.1:c.1579C= XP_011536179.1:p.His527=
XM_011537878.1:c.1579C= XP_011536180.1:p.His527=
XM_011537879.1:c.376C= XP_011536181.1:p.His126=
XM_011537880.1:c.1579C= XP_011536182.1:p.His527=
XM_011537881.1:c.1579C= XP_011536183.1:p.His527=
XM_011537882.1:c.1579C= XP_011536184.1:p.His527=
XM_005268629.4:c.1579C= XP_005268686.1:p.His527=
XM_011537877.3:c.1579C= XP_011536179.1:p.His527=
XM_011537881.3:c.1579C= XP_011536183.1:p.His527=
XM_011537882.3:c.1579C= XP_011536184.1:p.His527=
XM_017018786.2:c.1579C= XP_016874275.1:p.His527=
XM_017018789.2:c.1579C= XP_016874278.1:p.His527=
XM_024448833.1:c.376C= XP_024304601.1:p.His126=
XR_001748574.2:n.1821C=
NM_198578.4:c.1579C= MANE Select NP_940980.4:p.His527=