Canonical Allele Identifier: CA384413362

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757279A>C (hg19) ; chr12:g.40363477A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363477A>C , CM000674.2:g.40363477A>C	GRCh38
NC_000012.11:g.40757279A>C , CM000674.1:g.40757279A>C	GRCh37
NC_000012.10:g.39043546A>C	NCBI36
NG_011709.1:g.143467A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7104A>C MANE Select	ENSP00000298910.7:p.Gln2368His
ENST00000636518.1:c.901A>C
ENST00000679360.1:c.*6013A>C	ENSP00000505368.1:n.*6013A>C
ENST00000679532.1:c.2878A>C
ENST00000679683.1:c.894A>C
ENST00000680018.1:c.2549A>C	ENSP00000505347.1:n.2549A>C
ENST00000680422.1:c.4191A>C
ENST00000680425.1:c.2271A>C	ENSP00000506459.1:n.2271A>C
ENST00000680453.1:c.2561A>C
ENST00000680790.1:c.6849A>C	ENSP00000505335.1:p.Gln2283His
ENST00000681136.1:n.3088A>C
ENST00000681696.1:c.2787A>C	ENSP00000505871.1:p.Gln929His
ENST00000681773.1:n.311A>C
ENST00000298910.11:c.7104A>C	ENSP00000298910.7:p.Gln2368His
ENST00000430804.5:c.4400A>C
ENST00000479187.5:n.3785A>C
NM_198578.3:c.7104A>C	NP_940980.3:p.Gln2368His
XM_005268629.2:c.7104A>C	XP_005268686.1:p.Gln2368His
XM_011537877.1:c.7104A>C	XP_011536179.1:p.Gln2368His
XM_011537879.1:c.5901A>C	XP_011536181.1:p.Gln1967His
XR_944868.1:n.485-8650T>G
XM_005268629.4:c.7104A>C	XP_005268686.1:p.Gln2368His
XM_011537877.3:c.7104A>C	XP_011536179.1:p.Gln2368His
XM_017018787.1:c.4020A>C	XP_016874276.1:p.Gln1340His
XM_017018788.2:c.3366A>C	XP_016874277.1:p.Gln1122His
XM_024448833.1:c.5901A>C	XP_024304601.1:p.Gln1967His
XR_944868.2:n.485-8650T>G
NM_198578.4:c.7104A>C MANE Select	NP_940980.4:p.Gln2368His