Canonical Allele Identifier: CA2030937529

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40227018G= , CM000674.2:g.40227018G=	GRCh38
NC_000012.11:g.40620820G= , CM000674.1:g.40620820G=	GRCh37
NC_000012.10:g.38907087G=	NCBI36
NG_011709.1:g.7008G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.237+1378G= MANE Select	ENSP00000298910.7:n.237+1378G=
ENST00000644108.1:c.182-873G=
ENST00000679360.1:c.237+1378G=	ENSP00000505368.1:n.237+1378G=
ENST00000680235.1:n.392+1378G=
ENST00000680790.1:c.237+1378G=	ENSP00000505335.1:n.237+1378G=
ENST00000298910.11:c.237+1378G=	ENSP00000298910.7:n.237+1378G=
ENST00000343742.6:c.237+1378G=	ENSP00000341930.2:n.237+1378G=
ENST00000416796.5:c.24+1378G=	ENSP00000398726.1:n.24+1378G=
ENST00000474202.1:n.46+1378G=
NM_198578.3:c.237+1378G=	NP_940980.3:n.237+1378G=
XM_005268629.2:c.237+1378G=	XP_005268686.1:n.237+1378G=
XM_011537877.1:c.237+1378G=	XP_011536179.1:n.237+1378G=
XM_011537878.1:c.237+1378G=	XP_011536180.1:n.237+1378G=
XM_011537880.1:c.237+1378G=	XP_011536182.1:n.237+1378G=
XM_011537881.1:c.237+1378G=	XP_011536183.1:n.237+1378G=
XM_011537882.1:c.237+1378G=	XP_011536184.1:n.237+1378G=
XM_005268629.4:c.237+1378G=	XP_005268686.1:n.237+1378G=
XM_011537877.3:c.237+1378G=	XP_011536179.1:n.237+1378G=
XM_011537881.3:c.237+1378G=	XP_011536183.1:n.237+1378G=
XM_011537882.3:c.237+1378G=	XP_011536184.1:n.237+1378G=
XM_017018786.2:c.237+1378G=	XP_016874275.1:n.237+1378G=
XM_017018789.2:c.237+1378G=	XP_016874278.1:n.237+1378G=
XR_001748574.2:n.479+1378G=
NM_198578.4:c.237+1378G= MANE Select	NP_940980.4:n.237+1378G=