Canonical Allele Identifier: CA384413562
Gene: LRRK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.40757332T>C (hg19) chr12:g.40363530T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363530T>C , CM000674.2:g.40363530T>C GRCh38
NC_000012.11:g.40757332T>C , CM000674.1:g.40757332T>C GRCh37
NC_000012.10:g.39043599T>C NCBI36
NG_011709.1:g.143520T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7157T>C MANE Select ENSP00000298910.7:p.Leu2386Pro
ENST00000636518.1:c.954T>C
ENST00000679360.1:c.*6066T>C ENSP00000505368.1:n.*6066T>C
ENST00000679532.1:c.2931T>C
ENST00000679683.1:c.947T>C
ENST00000680018.1:c.2602T>C ENSP00000505347.1:n.2602T>C
ENST00000680422.1:c.4244T>C
ENST00000680425.1:c.2324T>C ENSP00000506459.1:n.2324T>C
ENST00000680453.1:c.2614T>C
ENST00000680790.1:c.6902T>C ENSP00000505335.1:p.Leu2301Pro
ENST00000681136.1:n.3141T>C
ENST00000681696.1:c.2840T>C ENSP00000505871.1:p.Leu947Pro
ENST00000681773.1:n.364T>C
ENST00000298910.11:c.7157T>C ENSP00000298910.7:p.Leu2386Pro
ENST00000430804.5:c.4453T>C
ENST00000479187.5:n.3838T>C
NM_198578.3:c.7157T>C NP_940980.3:p.Leu2386Pro
XM_005268629.2:c.7157T>C XP_005268686.1:p.Leu2386Pro
XM_011537877.1:c.7157T>C XP_011536179.1:p.Leu2386Pro
XM_011537879.1:c.5954T>C XP_011536181.1:p.Leu1985Pro
XR_944868.1:n.485-8703A>G
XM_005268629.4:c.7157T>C XP_005268686.1:p.Leu2386Pro
XM_011537877.3:c.7157T>C XP_011536179.1:p.Leu2386Pro
XM_017018787.1:c.4073T>C XP_016874276.1:p.Leu1358Pro
XM_017018788.2:c.3419T>C XP_016874277.1:p.Leu1140Pro
XM_024448833.1:c.5954T>C XP_024304601.1:p.Leu1985Pro
XR_944868.2:n.485-8703A>G
NM_198578.4:c.7157T>C MANE Select NP_940980.4:p.Leu2386Pro
Search 100 bp 5'
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