Canonical Allele Identifier: CA384407360

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745494C>G (hg19) ; chr12:g.40351692C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351692C>G , CM000674.2:g.40351692C>G	GRCh38
NC_000012.11:g.40745494C>G , CM000674.1:g.40745494C>G	GRCh37
NC_000012.10:g.39031761C>G	NCBI36
NG_011709.1:g.131682C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6535C>G MANE Select	ENSP00000298910.7:p.Leu2179Val
ENST00000636518.1:c.332C>G
ENST00000679360.1:c.*5444C>G	ENSP00000505368.1:n.*5444C>G
ENST00000679532.1:c.2309C>G
ENST00000679683.1:c.325C>G
ENST00000680018.1:c.1980C>G	ENSP00000505347.1:n.1980C>G
ENST00000680422.1:c.2180C>G
ENST00000680425.1:c.1702C>G	ENSP00000506459.1:n.1702C>G
ENST00000680453.1:c.1992C>G
ENST00000680790.1:c.6280C>G	ENSP00000505335.1:p.Leu2094Val
ENST00000681136.1:n.2519C>G
ENST00000681696.1:c.2218C>G	ENSP00000505871.1:p.Leu740Val
ENST00000298910.11:c.6535C>G	ENSP00000298910.7:p.Leu2179Val
ENST00000430804.5:c.3831C>G
ENST00000479187.5:n.3216C>G
NM_198578.3:c.6535C>G	NP_940980.3:p.Leu2179Val
XM_005268629.2:c.6535C>G	XP_005268686.1:p.Leu2179Val
XM_011537877.1:c.6535C>G	XP_011536179.1:p.Leu2179Val
XM_011537878.1:c.6535C>G	XP_011536180.1:p.Leu2179Val
XM_011537879.1:c.5332C>G	XP_011536181.1:p.Leu1778Val
XM_005268629.4:c.6535C>G	XP_005268686.1:p.Leu2179Val
XM_011537877.3:c.6535C>G	XP_011536179.1:p.Leu2179Val
XM_017018787.1:c.3451C>G	XP_016874276.1:p.Leu1151Val
XM_017018788.2:c.2797C>G	XP_016874277.1:p.Leu933Val
XM_024448833.1:c.5332C>G	XP_024304601.1:p.Leu1778Val
NM_198578.4:c.6535C>G MANE Select	NP_940980.4:p.Leu2179Val