Canonical Allele Identifier: CA2030983872

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40299125A= , CM000674.2:g.40299125A=	GRCh38
NC_000012.11:g.40692927A= , CM000674.1:g.40692927A=	GRCh37
NC_000012.10:g.38979194A=	NCBI36
NG_011709.1:g.79115A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.3364A= MANE Select	ENSP00000298910.7:p.Ile1122=
ENST00000679360.1:c.*2273A=	ENSP00000505368.1:n.*2273A=
ENST00000680790.1:c.3109A=	ENSP00000505335.1:p.Ile1037=
ENST00000298910.11:c.3364A=	ENSP00000298910.7:p.Ile1122=
ENST00000343742.6:c.3364A=	ENSP00000341930.2:p.Ile1122=
ENST00000430804.5:c.408A=
ENST00000479187.5:n.45A=
NM_198578.3:c.3364A=	NP_940980.3:p.Ile1122=
XM_005268629.2:c.3364A=	XP_005268686.1:p.Ile1122=
XM_011537877.1:c.3364A=	XP_011536179.1:p.Ile1122=
XM_011537878.1:c.3364A=	XP_011536180.1:p.Ile1122=
XM_011537879.1:c.2161A=	XP_011536181.1:p.Ile721=
XM_011537880.1:c.3364A=	XP_011536182.1:p.Ile1122=
XM_011537881.1:c.3364A=	XP_011536183.1:p.Ile1122=
XM_011537882.1:c.3364A=	XP_011536184.1:p.Ile1122=
XM_005268629.4:c.3364A=	XP_005268686.1:p.Ile1122=
XM_011537877.3:c.3364A=	XP_011536179.1:p.Ile1122=
XM_011537881.3:c.3364A=	XP_011536183.1:p.Ile1122=
XM_011537882.3:c.3364A=	XP_011536184.1:p.Ile1122=
XM_017018786.2:c.3364A=	XP_016874275.1:p.Ile1122=
XM_017018787.1:c.280A=	XP_016874276.1:p.Ile94=
XM_017018789.2:c.3364A=	XP_016874278.1:p.Ile1122=
XM_024448833.1:c.2161A=	XP_024304601.1:p.Ile721=
XR_001748574.2:n.3606A=
NM_198578.4:c.3364A= MANE Select	NP_940980.4:p.Ile1122=