Canonical Allele Identifier: CA384419662

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713917T>G (hg19) ; chr12:g.40320115T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320115T>G , CM000674.2:g.40320115T>G	GRCh38
NC_000012.11:g.40713917T>G , CM000674.1:g.40713917T>G	GRCh37
NC_000012.10:g.39000184T>G	NCBI36
NG_011709.1:g.100105T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4955T>G MANE Select	ENSP00000298910.7:p.Leu1652Arg
ENST00000679360.1:c.*3864T>G	ENSP00000505368.1:n.*3864T>G
ENST00000679532.1:c.729T>G
ENST00000680018.1:c.400T>G	ENSP00000505347.1:n.400T>G
ENST00000680422.1:c.600T>G
ENST00000680425.1:c.183-919T>G	ENSP00000506459.1:n.183-919T>G
ENST00000680453.1:c.473-919T>G
ENST00000680790.1:c.4700T>G	ENSP00000505335.1:p.Leu1567Arg
ENST00000681136.1:n.939T>G
ENST00000681696.1:c.638T>G	ENSP00000505871.1:p.Leu213Arg
ENST00000298910.11:c.4955T>G	ENSP00000298910.7:p.Leu1652Arg
ENST00000430804.5:c.2251T>G
ENST00000479187.5:n.1636T>G
NM_198578.3:c.4955T>G	NP_940980.3:p.Leu1652Arg
XM_005268629.2:c.4955T>G	XP_005268686.1:p.Leu1652Arg
XM_011537877.1:c.4955T>G	XP_011536179.1:p.Leu1652Arg
XM_011537878.1:c.4955T>G	XP_011536180.1:p.Leu1652Arg
XM_011537879.1:c.3752T>G	XP_011536181.1:p.Leu1251Arg
XM_011537881.1:c.4828-919T>G	XP_011536183.1:n.4828-919T>G
XM_005268629.4:c.4955T>G	XP_005268686.1:p.Leu1652Arg
XM_011537877.3:c.4955T>G	XP_011536179.1:p.Leu1652Arg
XM_011537881.3:c.4828-919T>G	XP_011536183.1:n.4828-919T>G
XM_017018787.1:c.1871T>G	XP_016874276.1:p.Leu624Arg
XM_017018788.2:c.1217T>G	XP_016874277.1:p.Leu406Arg
XM_024448833.1:c.3752T>G	XP_024304601.1:p.Leu1251Arg
XR_001748574.2:n.5323T>G
NM_198578.4:c.4955T>G MANE Select	NP_940980.4:p.Leu1652Arg