Canonical Allele Identifier: CA384403603

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734128A>G (hg19) ; chr12:g.40340326A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340326A>G , CM000674.2:g.40340326A>G	GRCh38
NC_000012.11:g.40734128A>G , CM000674.1:g.40734128A>G	GRCh37
NC_000012.10:g.39020395A>G	NCBI36
NG_011709.1:g.120316A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5981A>G MANE Select	ENSP00000298910.7:p.Asp1994Gly
ENST00000679360.1:c.*4890A>G	ENSP00000505368.1:n.*4890A>G
ENST00000679532.1:c.1755A>G
ENST00000680018.1:c.1426A>G	ENSP00000505347.1:n.1426A>G
ENST00000680422.1:c.1626A>G
ENST00000680425.1:c.1148A>G	ENSP00000506459.1:n.1148A>G
ENST00000680453.1:c.1438A>G
ENST00000680790.1:c.5726A>G	ENSP00000505335.1:p.Asp1909Gly
ENST00000681136.1:n.1965A>G
ENST00000681696.1:c.1664A>G	ENSP00000505871.1:p.Asp555Gly
ENST00000298910.11:c.5981A>G	ENSP00000298910.7:p.Asp1994Gly
ENST00000430804.5:c.3277A>G
ENST00000479187.5:n.2662A>G
NM_198578.3:c.5981A>G	NP_940980.3:p.Asp1994Gly
XM_005268629.2:c.5981A>G	XP_005268686.1:p.Asp1994Gly
XM_011537877.1:c.5981A>G	XP_011536179.1:p.Asp1994Gly
XM_011537878.1:c.5981A>G	XP_011536180.1:p.Asp1994Gly
XM_011537879.1:c.4778A>G	XP_011536181.1:p.Asp1593Gly
XM_005268629.4:c.5981A>G	XP_005268686.1:p.Asp1994Gly
XM_011537877.3:c.5981A>G	XP_011536179.1:p.Asp1994Gly
XM_017018787.1:c.2897A>G	XP_016874276.1:p.Asp966Gly
XM_017018788.2:c.2243A>G	XP_016874277.1:p.Asp748Gly
XM_024448833.1:c.4778A>G	XP_024304601.1:p.Asp1593Gly
NM_198578.4:c.5981A>G MANE Select	NP_940980.4:p.Asp1994Gly