Canonical Allele Identifier: CA384403881

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734180C>G (hg19) ; chr12:g.40340378C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340378C>G , CM000674.2:g.40340378C>G	GRCh38
NC_000012.11:g.40734180C>G , CM000674.1:g.40734180C>G	GRCh37
NC_000012.10:g.39020447C>G	NCBI36
NG_011709.1:g.120368C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6033C>G MANE Select	ENSP00000298910.7:p.Ile2011Met
ENST00000679360.1:c.*4942C>G	ENSP00000505368.1:n.*4942C>G
ENST00000679532.1:c.1807C>G
ENST00000680018.1:c.1478C>G	ENSP00000505347.1:n.1478C>G
ENST00000680422.1:c.1678C>G
ENST00000680425.1:c.1200C>G	ENSP00000506459.1:n.1200C>G
ENST00000680453.1:c.1490C>G
ENST00000680790.1:c.5778C>G	ENSP00000505335.1:p.Ile1926Met
ENST00000681136.1:n.2017C>G
ENST00000681696.1:c.1716C>G	ENSP00000505871.1:p.Ile572Met
ENST00000298910.11:c.6033C>G	ENSP00000298910.7:p.Ile2011Met
ENST00000430804.5:c.3329C>G
ENST00000479187.5:n.2714C>G
NM_198578.3:c.6033C>G	NP_940980.3:p.Ile2011Met
XM_005268629.2:c.6033C>G	XP_005268686.1:p.Ile2011Met
XM_011537877.1:c.6033C>G	XP_011536179.1:p.Ile2011Met
XM_011537878.1:c.6033C>G	XP_011536180.1:p.Ile2011Met
XM_011537879.1:c.4830C>G	XP_011536181.1:p.Ile1610Met
XM_005268629.4:c.6033C>G	XP_005268686.1:p.Ile2011Met
XM_011537877.3:c.6033C>G	XP_011536179.1:p.Ile2011Met
XM_017018787.1:c.2949C>G	XP_016874276.1:p.Ile983Met
XM_017018788.2:c.2295C>G	XP_016874277.1:p.Ile765Met
XM_024448833.1:c.4830C>G	XP_024304601.1:p.Ile1610Met
NM_198578.4:c.6033C>G MANE Select	NP_940980.4:p.Ile2011Met