Canonical Allele Identifier: CA384420986

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40716980C>G (hg19) ; chr12:g.40323178C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323178C>G , CM000674.2:g.40323178C>G	GRCh38
NC_000012.11:g.40716980C>G , CM000674.1:g.40716980C>G	GRCh37
NC_000012.10:g.39003247C>G	NCBI36
NG_011709.1:g.103168C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5528C>G MANE Select	ENSP00000298910.7:p.Pro1843Arg
ENST00000679360.1:c.*4437C>G	ENSP00000505368.1:n.*4437C>G
ENST00000679532.1:c.1302C>G
ENST00000680018.1:c.973C>G	ENSP00000505347.1:n.973C>G
ENST00000680422.1:c.1173C>G
ENST00000680425.1:c.695C>G	ENSP00000506459.1:n.695C>G
ENST00000680453.1:c.985C>G
ENST00000680790.1:c.5273C>G	ENSP00000505335.1:p.Pro1758Arg
ENST00000681136.1:n.1512C>G
ENST00000681696.1:c.1211C>G	ENSP00000505871.1:p.Pro404Arg
ENST00000298910.11:c.5528C>G	ENSP00000298910.7:p.Pro1843Arg
ENST00000430804.5:c.2824C>G
ENST00000479187.5:n.2209C>G
NM_198578.3:c.5528C>G	NP_940980.3:p.Pro1843Arg
XM_005268629.2:c.5528C>G	XP_005268686.1:p.Pro1843Arg
XM_011537877.1:c.5528C>G	XP_011536179.1:p.Pro1843Arg
XM_011537878.1:c.5528C>G	XP_011536180.1:p.Pro1843Arg
XM_011537879.1:c.4325C>G	XP_011536181.1:p.Pro1442Arg
XM_005268629.4:c.5528C>G	XP_005268686.1:p.Pro1843Arg
XM_011537877.3:c.5528C>G	XP_011536179.1:p.Pro1843Arg
XM_017018787.1:c.2444C>G	XP_016874276.1:p.Pro815Arg
XM_017018788.2:c.1790C>G	XP_016874277.1:p.Pro597Arg
XM_024448833.1:c.4325C>G	XP_024304601.1:p.Pro1442Arg
NM_198578.4:c.5528C>G MANE Select	NP_940980.4:p.Pro1843Arg