Canonical Allele Identifier: CA479267968

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713849A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320047A>G , CM000674.2:g.40320047A>G	GRCh38
NC_000012.11:g.40713849A>G , CM000674.1:g.40713849A>G	GRCh37
NC_000012.10:g.39000116A>G	NCBI36
NG_011709.1:g.100037A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4887A>G MANE Select	ENSP00000298910.7:p.Arg1629=
ENST00000679360.1:c.*3796A>G	ENSP00000505368.1:n.*3796A>G
ENST00000679532.1:c.661A>G
ENST00000680018.1:c.332A>G	ENSP00000505347.1:n.332A>G
ENST00000680422.1:c.532A>G
ENST00000680425.1:c.183-987A>G	ENSP00000506459.1:n.183-987A>G
ENST00000680453.1:c.473-987A>G
ENST00000680790.1:c.4632A>G	ENSP00000505335.1:p.Arg1544=
ENST00000681136.1:n.871A>G
ENST00000681696.1:c.570A>G	ENSP00000505871.1:p.Arg190=
ENST00000298910.11:c.4887A>G	ENSP00000298910.7:p.Arg1629=
ENST00000430804.5:c.2183A>G
ENST00000479187.5:n.1568A>G
ENST00000481256.1:n.546A>G
NM_198578.3:c.4887A>G	NP_940980.3:p.Arg1629=
XM_005268629.2:c.4887A>G	XP_005268686.1:p.Arg1629=
XM_011537877.1:c.4887A>G	XP_011536179.1:p.Arg1629=
XM_011537878.1:c.4887A>G	XP_011536180.1:p.Arg1629=
XM_011537879.1:c.3684A>G	XP_011536181.1:p.Arg1228=
XM_011537881.1:c.4828-987A>G	XP_011536183.1:n.4828-987A>G
XM_005268629.4:c.4887A>G	XP_005268686.1:p.Arg1629=
XM_011537877.3:c.4887A>G	XP_011536179.1:p.Arg1629=
XM_011537881.3:c.4828-987A>G	XP_011536183.1:n.4828-987A>G
XM_017018787.1:c.1803A>G	XP_016874276.1:p.Arg601=
XM_017018788.2:c.1149A>G	XP_016874277.1:p.Arg383=
XM_024448833.1:c.3684A>G	XP_024304601.1:p.Arg1228=
XR_001748574.2:n.5255A>G
NM_198578.4:c.4887A>G MANE Select	NP_940980.4:p.Arg1629=