Canonical Allele Identifier: CA6513869
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs758901246

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298481T>C , CM000674.2:g.40298481T>C GRCh38
NC_000012.11:g.40692283T>C , CM000674.1:g.40692283T>C GRCh37
NC_000012.10:g.38978550T>C NCBI36
NG_011709.1:g.78471T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3335T>C MANE Select ENSP00000298910.7:p.Leu1112Pro
ENST00000679360.1:c.*2244T>C ENSP00000505368.1:n.*2244T>C
ENST00000680790.1:c.3080T>C ENSP00000505335.1:p.Leu1027Pro
ENST00000298910.11:c.3335T>C ENSP00000298910.7:p.Leu1112Pro
ENST00000343742.6:c.3335T>C ENSP00000341930.2:p.Leu1112Pro
ENST00000430804.5:c.379T>C
ENST00000479187.5:n.16T>C
NM_198578.3:c.3335T>C NP_940980.3:p.Leu1112Pro
XM_005268629.2:c.3335T>C XP_005268686.1:p.Leu1112Pro
XM_011537877.1:c.3335T>C XP_011536179.1:p.Leu1112Pro
XM_011537878.1:c.3335T>C XP_011536180.1:p.Leu1112Pro
XM_011537879.1:c.2132T>C XP_011536181.1:p.Leu711Pro
XM_011537880.1:c.3335T>C XP_011536182.1:p.Leu1112Pro
XM_011537881.1:c.3335T>C XP_011536183.1:p.Leu1112Pro
XM_011537882.1:c.3335T>C XP_011536184.1:p.Leu1112Pro
XM_005268629.4:c.3335T>C XP_005268686.1:p.Leu1112Pro
XM_011537877.3:c.3335T>C XP_011536179.1:p.Leu1112Pro
XM_011537881.3:c.3335T>C XP_011536183.1:p.Leu1112Pro
XM_011537882.3:c.3335T>C XP_011536184.1:p.Leu1112Pro
XM_017018786.2:c.3335T>C XP_016874275.1:p.Leu1112Pro
XM_017018787.1:c.251T>C XP_016874276.1:p.Leu84Pro
XM_017018789.2:c.3335T>C XP_016874278.1:p.Leu1112Pro
XM_024448833.1:c.2132T>C XP_024304601.1:p.Leu711Pro
XR_001748574.2:n.3577T>C
NM_198578.4:c.3335T>C MANE Select NP_940980.4:p.Leu1112Pro