Canonical Allele Identifier: CA2030983095
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298805_40298806delinsTG , CM000674.2:g.40298805_40298806delinsTG GRCh38
NC_000012.11:g.40692607_40692608delinsTG , CM000674.1:g.40692607_40692608delinsTG GRCh37
NC_000012.10:g.38978874_38978875delinsTG NCBI36
NG_011709.1:g.78795_78796delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3348-304_3348-303delinsTG MANE Select ENSP00000298910.7:n.3348-304_3348-303delinsTG
ENST00000679360.1:c.*2257-304_*2257-303delinsTG ENSP00000505368.1:n.*2257-304_*2257-303delinsTG
ENST00000680790.1:c.3093-304_3093-303delinsTG ENSP00000505335.1:n.3093-304_3093-303delinsTG
ENST00000298910.11:c.3348-304_3348-303delinsTG ENSP00000298910.7:n.3348-304_3348-303delinsTG
ENST00000343742.6:c.3348-304_3348-303delinsTG ENSP00000341930.2:n.3348-304_3348-303delinsTG
ENST00000430804.5:c.392-304_392-303delinsTG
ENST00000479187.5:n.29-304_29-303delinsTG
NM_198578.3:c.3348-304_3348-303delinsTG NP_940980.3:n.3348-304_3348-303delinsTG
XM_005268629.2:c.3348-304_3348-303delinsTG XP_005268686.1:n.3348-304_3348-303delinsTG
XM_011537877.1:c.3348-304_3348-303delinsTG XP_011536179.1:n.3348-304_3348-303delinsTG
XM_011537878.1:c.3348-304_3348-303delinsTG XP_011536180.1:n.3348-304_3348-303delinsTG
XM_011537879.1:c.2145-304_2145-303delinsTG XP_011536181.1:n.2145-304_2145-303delinsTG
XM_011537880.1:c.3348-304_3348-303delinsTG XP_011536182.1:n.3348-304_3348-303delinsTG
XM_011537881.1:c.3348-304_3348-303delinsTG XP_011536183.1:n.3348-304_3348-303delinsTG
XM_011537882.1:c.3348-304_3348-303delinsTG XP_011536184.1:n.3348-304_3348-303delinsTG
XM_005268629.4:c.3348-304_3348-303delinsTG XP_005268686.1:n.3348-304_3348-303delinsTG
XM_011537877.3:c.3348-304_3348-303delinsTG XP_011536179.1:n.3348-304_3348-303delinsTG
XM_011537881.3:c.3348-304_3348-303delinsTG XP_011536183.1:n.3348-304_3348-303delinsTG
XM_011537882.3:c.3348-304_3348-303delinsTG XP_011536184.1:n.3348-304_3348-303delinsTG
XM_017018786.2:c.3348-304_3348-303delinsTG XP_016874275.1:n.3348-304_3348-303delinsTG
XM_017018787.1:c.264-304_264-303delinsTG XP_016874276.1:n.264-304_264-303delinsTG
XM_017018789.2:c.3348-304_3348-303delinsTG XP_016874278.1:n.3348-304_3348-303delinsTG
XM_024448833.1:c.2145-304_2145-303delinsTG XP_024304601.1:n.2145-304_2145-303delinsTG
XR_001748574.2:n.3590-304_3590-303delinsTG
NM_198578.4:c.3348-304_3348-303delinsTG MANE Select NP_940980.4:n.3348-304_3348-303delinsTG