Canonical Allele Identifier: CA2030897731
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40252998A= , CM000674.2:g.40252998A= GRCh38
NC_000012.11:g.40646800A= , CM000674.1:g.40646800A= GRCh37
NC_000012.10:g.38933067A= NCBI36
NG_011709.1:g.32988A=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.1270A= MANE Select ENSP00000298910.7:p.Thr424=
ENST00000679360.1:c.*179A= ENSP00000505368.1:n.*179A=
ENST00000680790.1:c.1270A= ENSP00000505335.1:p.Thr424=
ENST00000298910.11:c.1270A= ENSP00000298910.7:p.Thr424=
ENST00000343742.6:c.1270A= ENSP00000341930.2:p.Thr424=
ENST00000416796.5:c.644A= ENSP00000398726.1:p.Asn215=
NM_198578.3:c.1270A= NP_940980.3:p.Thr424=
XM_005268629.2:c.1270A= XP_005268686.1:p.Thr424=
XM_011537877.1:c.1270A= XP_011536179.1:p.Thr424=
XM_011537878.1:c.1270A= XP_011536180.1:p.Thr424=
XM_011537879.1:c.67A= XP_011536181.1:p.Thr23=
XM_011537880.1:c.1270A= XP_011536182.1:p.Thr424=
XM_011537881.1:c.1270A= XP_011536183.1:p.Thr424=
XM_011537882.1:c.1270A= XP_011536184.1:p.Thr424=
XM_005268629.4:c.1270A= XP_005268686.1:p.Thr424=
XM_011537877.3:c.1270A= XP_011536179.1:p.Thr424=
XM_011537881.3:c.1270A= XP_011536183.1:p.Thr424=
XM_011537882.3:c.1270A= XP_011536184.1:p.Thr424=
XM_017018786.2:c.1270A= XP_016874275.1:p.Thr424=
XM_017018789.2:c.1270A= XP_016874278.1:p.Thr424=
XM_024448833.1:c.67A= XP_024304601.1:p.Thr23=
XR_001748574.2:n.1512A=
NM_198578.4:c.1270A= MANE Select NP_940980.4:p.Thr424=