Canonical Allele Identifier: CA2030982812
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298376A= , CM000674.2:g.40298376A= GRCh38
NC_000012.11:g.40692178A= , CM000674.1:g.40692178A= GRCh37
NC_000012.10:g.38978445A= NCBI36
NG_011709.1:g.78366A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3230A= MANE Select ENSP00000298910.7:p.Asp1077=
ENST00000679360.1:c.*2139A= ENSP00000505368.1:n.*2139A=
ENST00000680790.1:c.2975A= ENSP00000505335.1:p.Asp992=
ENST00000298910.11:c.3230A= ENSP00000298910.7:p.Asp1077=
ENST00000343742.6:c.3230A= ENSP00000341930.2:p.Asp1077=
ENST00000430804.5:c.274A=
NM_198578.3:c.3230A= NP_940980.3:p.Asp1077=
XM_005268629.2:c.3230A= XP_005268686.1:p.Asp1077=
XM_011537877.1:c.3230A= XP_011536179.1:p.Asp1077=
XM_011537878.1:c.3230A= XP_011536180.1:p.Asp1077=
XM_011537879.1:c.2027A= XP_011536181.1:p.Asp676=
XM_011537880.1:c.3230A= XP_011536182.1:p.Asp1077=
XM_011537881.1:c.3230A= XP_011536183.1:p.Asp1077=
XM_011537882.1:c.3230A= XP_011536184.1:p.Asp1077=
XM_005268629.4:c.3230A= XP_005268686.1:p.Asp1077=
XM_011537877.3:c.3230A= XP_011536179.1:p.Asp1077=
XM_011537881.3:c.3230A= XP_011536183.1:p.Asp1077=
XM_011537882.3:c.3230A= XP_011536184.1:p.Asp1077=
XM_017018786.2:c.3230A= XP_016874275.1:p.Asp1077=
XM_017018787.1:c.146A= XP_016874276.1:p.Asp49=
XM_017018789.2:c.3230A= XP_016874278.1:p.Asp1077=
XM_024448833.1:c.2027A= XP_024304601.1:p.Asp676=
XR_001748574.2:n.3472A=
NM_198578.4:c.3230A= MANE Select NP_940980.4:p.Asp1077=