Canonical Allele Identifier: CA384413287

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757259G>A (hg19) ; chr12:g.40363457G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363457G>A , CM000674.2:g.40363457G>A	GRCh38
NC_000012.11:g.40757259G>A , CM000674.1:g.40757259G>A	GRCh37
NC_000012.10:g.39043526G>A	NCBI36
NG_011709.1:g.143447G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7084G>A MANE Select	ENSP00000298910.7:p.Ala2362Thr
ENST00000636518.1:c.881G>A
ENST00000679360.1:c.*5993G>A	ENSP00000505368.1:n.*5993G>A
ENST00000679532.1:c.2858G>A
ENST00000679683.1:c.874G>A
ENST00000680018.1:c.2529G>A	ENSP00000505347.1:n.2529G>A
ENST00000680422.1:c.4171G>A
ENST00000680425.1:c.2251G>A	ENSP00000506459.1:n.2251G>A
ENST00000680453.1:c.2541G>A
ENST00000680790.1:c.6829G>A	ENSP00000505335.1:p.Ala2277Thr
ENST00000681136.1:n.3068G>A
ENST00000681696.1:c.2767G>A	ENSP00000505871.1:p.Ala923Thr
ENST00000681773.1:n.291G>A
ENST00000298910.11:c.7084G>A	ENSP00000298910.7:p.Ala2362Thr
ENST00000430804.5:c.4380G>A
ENST00000479187.5:n.3765G>A
NM_198578.3:c.7084G>A	NP_940980.3:p.Ala2362Thr
XM_005268629.2:c.7084G>A	XP_005268686.1:p.Ala2362Thr
XM_011537877.1:c.7084G>A	XP_011536179.1:p.Ala2362Thr
XM_011537879.1:c.5881G>A	XP_011536181.1:p.Ala1961Thr
XR_944868.1:n.485-8630C>T
XM_005268629.4:c.7084G>A	XP_005268686.1:p.Ala2362Thr
XM_011537877.3:c.7084G>A	XP_011536179.1:p.Ala2362Thr
XM_017018787.1:c.4000G>A	XP_016874276.1:p.Ala1334Thr
XM_017018788.2:c.3346G>A	XP_016874277.1:p.Ala1116Thr
XM_024448833.1:c.5881G>A	XP_024304601.1:p.Ala1961Thr
XR_944868.2:n.485-8630C>T
NM_198578.4:c.7084G>A MANE Select	NP_940980.4:p.Ala2362Thr