Canonical Allele Identifier: CA384413335

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757271G>A (hg19) ; chr12:g.40363469G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363469G>A , CM000674.2:g.40363469G>A	GRCh38
NC_000012.11:g.40757271G>A , CM000674.1:g.40757271G>A	GRCh37
NC_000012.10:g.39043538G>A	NCBI36
NG_011709.1:g.143459G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7096G>A MANE Select	ENSP00000298910.7:p.Ala2366Thr
ENST00000636518.1:c.893G>A
ENST00000679360.1:c.*6005G>A	ENSP00000505368.1:n.*6005G>A
ENST00000679532.1:c.2870G>A
ENST00000679683.1:c.886G>A
ENST00000680018.1:c.2541G>A	ENSP00000505347.1:n.2541G>A
ENST00000680422.1:c.4183G>A
ENST00000680425.1:c.2263G>A	ENSP00000506459.1:n.2263G>A
ENST00000680453.1:c.2553G>A
ENST00000680790.1:c.6841G>A	ENSP00000505335.1:p.Ala2281Thr
ENST00000681136.1:n.3080G>A
ENST00000681696.1:c.2779G>A	ENSP00000505871.1:p.Ala927Thr
ENST00000681773.1:n.303G>A
ENST00000298910.11:c.7096G>A	ENSP00000298910.7:p.Ala2366Thr
ENST00000430804.5:c.4392G>A
ENST00000479187.5:n.3777G>A
NM_198578.3:c.7096G>A	NP_940980.3:p.Ala2366Thr
XM_005268629.2:c.7096G>A	XP_005268686.1:p.Ala2366Thr
XM_011537877.1:c.7096G>A	XP_011536179.1:p.Ala2366Thr
XM_011537879.1:c.5893G>A	XP_011536181.1:p.Ala1965Thr
XR_944868.1:n.485-8642C>T
XM_005268629.4:c.7096G>A	XP_005268686.1:p.Ala2366Thr
XM_011537877.3:c.7096G>A	XP_011536179.1:p.Ala2366Thr
XM_017018787.1:c.4012G>A	XP_016874276.1:p.Ala1338Thr
XM_017018788.2:c.3358G>A	XP_016874277.1:p.Ala1120Thr
XM_024448833.1:c.5893G>A	XP_024304601.1:p.Ala1965Thr
XR_944868.2:n.485-8642C>T
NM_198578.4:c.7096G>A MANE Select	NP_940980.4:p.Ala2366Thr