Canonical Allele Identifier: CA479236902

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40263808-G-A
• MyVariant Identifiers: chr12:g.40657610G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40263808G>A , CM000674.2:g.40263808G>A	GRCh38
NC_000012.11:g.40657610G>A , CM000674.1:g.40657610G>A	GRCh37
NC_000012.10:g.38943877G>A	NCBI36
NG_011709.1:g.43798G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.1563G>A MANE Select	ENSP00000298910.7:p.Arg521=
ENST00000679360.1:c.*472G>A	ENSP00000505368.1:n.*472G>A
ENST00000680790.1:c.1308G>A	ENSP00000505335.1:p.Arg436=
ENST00000298910.11:c.1563G>A	ENSP00000298910.7:p.Arg521=
ENST00000343742.6:c.1563G>A	ENSP00000341930.2:p.Arg521=
ENST00000416796.5:c.807G>A	ENSP00000398726.1:p.Arg269=
NM_198578.3:c.1563G>A	NP_940980.3:p.Arg521=
XM_005268629.2:c.1563G>A	XP_005268686.1:p.Arg521=
XM_011537877.1:c.1563G>A	XP_011536179.1:p.Arg521=
XM_011537878.1:c.1563G>A	XP_011536180.1:p.Arg521=
XM_011537879.1:c.360G>A	XP_011536181.1:p.Arg120=
XM_011537880.1:c.1563G>A	XP_011536182.1:p.Arg521=
XM_011537881.1:c.1563G>A	XP_011536183.1:p.Arg521=
XM_011537882.1:c.1563G>A	XP_011536184.1:p.Arg521=
XM_005268629.4:c.1563G>A	XP_005268686.1:p.Arg521=
XM_011537877.3:c.1563G>A	XP_011536179.1:p.Arg521=
XM_011537881.3:c.1563G>A	XP_011536183.1:p.Arg521=
XM_011537882.3:c.1563G>A	XP_011536184.1:p.Arg521=
XM_017018786.2:c.1563G>A	XP_016874275.1:p.Arg521=
XM_017018789.2:c.1563G>A	XP_016874278.1:p.Arg521=
XM_024448833.1:c.360G>A	XP_024304601.1:p.Arg120=
XR_001748574.2:n.1805G>A
NM_198578.4:c.1563G>A MANE Select	NP_940980.4:p.Arg521=