Canonical Allele Identifier: CA384419723

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713944C>G (hg19) ; chr12:g.40320142C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320142C>G , CM000674.2:g.40320142C>G	GRCh38
NC_000012.11:g.40713944C>G , CM000674.1:g.40713944C>G	GRCh37
NC_000012.10:g.39000211C>G	NCBI36
NG_011709.1:g.100132C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4982C>G MANE Select	ENSP00000298910.7:p.Pro1661Arg
ENST00000679360.1:c.*3891C>G	ENSP00000505368.1:n.*3891C>G
ENST00000679532.1:c.756C>G
ENST00000680018.1:c.427C>G	ENSP00000505347.1:n.427C>G
ENST00000680422.1:c.627C>G
ENST00000680425.1:c.183-892C>G	ENSP00000506459.1:n.183-892C>G
ENST00000680453.1:c.473-892C>G
ENST00000680790.1:c.4727C>G	ENSP00000505335.1:p.Pro1576Arg
ENST00000681136.1:n.966C>G
ENST00000681696.1:c.665C>G	ENSP00000505871.1:p.Pro222Arg
ENST00000298910.11:c.4982C>G	ENSP00000298910.7:p.Pro1661Arg
ENST00000430804.5:c.2278C>G
ENST00000479187.5:n.1663C>G
NM_198578.3:c.4982C>G	NP_940980.3:p.Pro1661Arg
XM_005268629.2:c.4982C>G	XP_005268686.1:p.Pro1661Arg
XM_011537877.1:c.4982C>G	XP_011536179.1:p.Pro1661Arg
XM_011537878.1:c.4982C>G	XP_011536180.1:p.Pro1661Arg
XM_011537879.1:c.3779C>G	XP_011536181.1:p.Pro1260Arg
XM_011537881.1:c.4828-892C>G	XP_011536183.1:n.4828-892C>G
XM_005268629.4:c.4982C>G	XP_005268686.1:p.Pro1661Arg
XM_011537877.3:c.4982C>G	XP_011536179.1:p.Pro1661Arg
XM_011537881.3:c.4828-892C>G	XP_011536183.1:n.4828-892C>G
XM_017018787.1:c.1898C>G	XP_016874276.1:p.Pro633Arg
XM_017018788.2:c.1244C>G	XP_016874277.1:p.Pro415Arg
XM_024448833.1:c.3779C>G	XP_024304601.1:p.Pro1260Arg
XR_001748574.2:n.5350C>G
NM_198578.4:c.4982C>G MANE Select	NP_940980.4:p.Pro1661Arg