Canonical Allele Identifier: CA384403998
Gene: LRRK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.40734208G>C (hg19) chr12:g.40340406G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340406G>C , CM000674.2:g.40340406G>C GRCh38
NC_000012.11:g.40734208G>C , CM000674.1:g.40734208G>C GRCh37
NC_000012.10:g.39020475G>C NCBI36
NG_011709.1:g.120396G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.6061G>C MANE Select ENSP00000298910.7:p.Ala2021Pro
ENST00000679360.1:c.*4970G>C ENSP00000505368.1:n.*4970G>C
ENST00000679532.1:c.1835G>C
ENST00000680018.1:c.1506G>C ENSP00000505347.1:n.1506G>C
ENST00000680422.1:c.1706G>C
ENST00000680425.1:c.1228G>C ENSP00000506459.1:n.1228G>C
ENST00000680453.1:c.1518G>C
ENST00000680790.1:c.5806G>C ENSP00000505335.1:p.Ala1936Pro
ENST00000681136.1:n.2045G>C
ENST00000681696.1:c.1744G>C ENSP00000505871.1:p.Ala582Pro
ENST00000298910.11:c.6061G>C ENSP00000298910.7:p.Ala2021Pro
ENST00000430804.5:c.3357G>C
ENST00000479187.5:n.2742G>C
NM_198578.3:c.6061G>C NP_940980.3:p.Ala2021Pro
XM_005268629.2:c.6061G>C XP_005268686.1:p.Ala2021Pro
XM_011537877.1:c.6061G>C XP_011536179.1:p.Ala2021Pro
XM_011537878.1:c.6061G>C XP_011536180.1:p.Ala2021Pro
XM_011537879.1:c.4858G>C XP_011536181.1:p.Ala1620Pro
XM_005268629.4:c.6061G>C XP_005268686.1:p.Ala2021Pro
XM_011537877.3:c.6061G>C XP_011536179.1:p.Ala2021Pro
XM_017018787.1:c.2977G>C XP_016874276.1:p.Ala993Pro
XM_017018788.2:c.2323G>C XP_016874277.1:p.Ala775Pro
XM_024448833.1:c.4858G>C XP_024304601.1:p.Ala1620Pro
NM_198578.4:c.6061G>C MANE Select NP_940980.4:p.Ala2021Pro
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