Canonical Allele Identifier: CA2030937658
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40227114_40227116delinsTAG , CM000674.2:g.40227114_40227116delinsTAG GRCh38
NC_000012.11:g.40620916_40620918delinsTAG , CM000674.1:g.40620916_40620918delinsTAG GRCh37
NC_000012.10:g.38907183_38907185delinsTAG NCBI36
NG_011709.1:g.7104_7106delinsTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.237+1474_237+1476delinsTAG MANE Select ENSP00000298910.7:n.237+1474_237+1476delinsTAG
ENST00000644108.1:c.182-777_182-775delinsTAG
ENST00000679360.1:c.237+1474_237+1476delinsTAG ENSP00000505368.1:n.237+1474_237+1476delinsTAG
ENST00000680235.1:n.392+1474_392+1476delinsTAG
ENST00000680790.1:c.237+1474_237+1476delinsTAG ENSP00000505335.1:n.237+1474_237+1476delinsTAG
ENST00000298910.11:c.237+1474_237+1476delinsTAG ENSP00000298910.7:n.237+1474_237+1476delinsTAG
ENST00000343742.6:c.237+1474_237+1476delinsTAG ENSP00000341930.2:n.237+1474_237+1476delinsTAG
ENST00000416796.5:c.24+1474_24+1476delinsTAG ENSP00000398726.1:n.24+1474_24+1476delinsTAG
ENST00000474202.1:n.46+1474_46+1476delinsTAG
NM_198578.3:c.237+1474_237+1476delinsTAG NP_940980.3:n.237+1474_237+1476delinsTAG
XM_005268629.2:c.237+1474_237+1476delinsTAG XP_005268686.1:n.237+1474_237+1476delinsTAG
XM_011537877.1:c.237+1474_237+1476delinsTAG XP_011536179.1:n.237+1474_237+1476delinsTAG
XM_011537878.1:c.237+1474_237+1476delinsTAG XP_011536180.1:n.237+1474_237+1476delinsTAG
XM_011537880.1:c.237+1474_237+1476delinsTAG XP_011536182.1:n.237+1474_237+1476delinsTAG
XM_011537881.1:c.237+1474_237+1476delinsTAG XP_011536183.1:n.237+1474_237+1476delinsTAG
XM_011537882.1:c.237+1474_237+1476delinsTAG XP_011536184.1:n.237+1474_237+1476delinsTAG
XM_005268629.4:c.237+1474_237+1476delinsTAG XP_005268686.1:n.237+1474_237+1476delinsTAG
XM_011537877.3:c.237+1474_237+1476delinsTAG XP_011536179.1:n.237+1474_237+1476delinsTAG
XM_011537881.3:c.237+1474_237+1476delinsTAG XP_011536183.1:n.237+1474_237+1476delinsTAG
XM_011537882.3:c.237+1474_237+1476delinsTAG XP_011536184.1:n.237+1474_237+1476delinsTAG
XM_017018786.2:c.237+1474_237+1476delinsTAG XP_016874275.1:n.237+1474_237+1476delinsTAG
XM_017018789.2:c.237+1474_237+1476delinsTAG XP_016874278.1:n.237+1474_237+1476delinsTAG
XR_001748574.2:n.479+1474_479+1476delinsTAG
NM_198578.4:c.237+1474_237+1476delinsTAG MANE Select NP_940980.4:n.237+1474_237+1476delinsTAG