Canonical Allele Identifier: CA384403979
Gene: LRRK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.40734202G>C (hg19) chr12:g.40340400G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340400G>C , CM000674.2:g.40340400G>C GRCh38
NC_000012.11:g.40734202G>C , CM000674.1:g.40734202G>C GRCh37
NC_000012.10:g.39020469G>C NCBI36
NG_011709.1:g.120390G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.6055G>C MANE Select ENSP00000298910.7:p.Gly2019Arg
ENST00000679360.1:c.*4964G>C ENSP00000505368.1:n.*4964G>C
ENST00000679532.1:c.1829G>C
ENST00000680018.1:c.1500G>C ENSP00000505347.1:n.1500G>C
ENST00000680422.1:c.1700G>C
ENST00000680425.1:c.1222G>C ENSP00000506459.1:n.1222G>C
ENST00000680453.1:c.1512G>C
ENST00000680790.1:c.5800G>C ENSP00000505335.1:p.Gly1934Arg
ENST00000681136.1:n.2039G>C
ENST00000681696.1:c.1738G>C ENSP00000505871.1:p.Gly580Arg
ENST00000298910.11:c.6055G>C ENSP00000298910.7:p.Gly2019Arg
ENST00000430804.5:c.3351G>C
ENST00000479187.5:n.2736G>C
NM_198578.3:c.6055G>C NP_940980.3:p.Gly2019Arg
XM_005268629.2:c.6055G>C XP_005268686.1:p.Gly2019Arg
XM_011537877.1:c.6055G>C XP_011536179.1:p.Gly2019Arg
XM_011537878.1:c.6055G>C XP_011536180.1:p.Gly2019Arg
XM_011537879.1:c.4852G>C XP_011536181.1:p.Gly1618Arg
XM_005268629.4:c.6055G>C XP_005268686.1:p.Gly2019Arg
XM_011537877.3:c.6055G>C XP_011536179.1:p.Gly2019Arg
XM_017018787.1:c.2971G>C XP_016874276.1:p.Gly991Arg
XM_017018788.2:c.2317G>C XP_016874277.1:p.Gly773Arg
XM_024448833.1:c.4852G>C XP_024304601.1:p.Gly1618Arg
NM_198578.4:c.6055G>C MANE Select NP_940980.4:p.Gly2019Arg
Search 100 bp 5'
Search 100 bp 3'