Canonical Allele Identifier: CA2030984057

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40299224G= , CM000674.2:g.40299224G=	GRCh38
NC_000012.11:g.40693026G= , CM000674.1:g.40693026G=	GRCh37
NC_000012.10:g.38979293G=	NCBI36
NG_011709.1:g.79214G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3463G= MANE Select	ENSP00000298910.7:p.Val1155=
ENST00000679360.1:c.*2372G=	ENSP00000505368.1:n.*2372G=
ENST00000680790.1:c.3208G=	ENSP00000505335.1:p.Val1070=
ENST00000298910.11:c.3463G=	ENSP00000298910.7:p.Val1155=
ENST00000343742.6:c.3463G=	ENSP00000341930.2:p.Val1155=
ENST00000430804.5:c.507G=
ENST00000479187.5:n.144G=
NM_198578.3:c.3463G=	NP_940980.3:p.Val1155=
XM_005268629.2:c.3463G=	XP_005268686.1:p.Val1155=
XM_011537877.1:c.3463G=	XP_011536179.1:p.Val1155=
XM_011537878.1:c.3463G=	XP_011536180.1:p.Val1155=
XM_011537879.1:c.2260G=	XP_011536181.1:p.Val754=
XM_011537880.1:c.3463G=	XP_011536182.1:p.Val1155=
XM_011537881.1:c.3463G=	XP_011536183.1:p.Val1155=
XM_011537882.1:c.3463G=	XP_011536184.1:p.Val1155=
XM_005268629.4:c.3463G=	XP_005268686.1:p.Val1155=
XM_011537877.3:c.3463G=	XP_011536179.1:p.Val1155=
XM_011537881.3:c.3463G=	XP_011536183.1:p.Val1155=
XM_011537882.3:c.3463G=	XP_011536184.1:p.Val1155=
XM_017018786.2:c.3463G=	XP_016874275.1:p.Val1155=
XM_017018787.1:c.379G=	XP_016874276.1:p.Val127=
XM_017018789.2:c.3463G=	XP_016874278.1:p.Val1155=
XM_024448833.1:c.2260G=	XP_024304601.1:p.Val754=
XR_001748574.2:n.3705G=
NM_198578.4:c.3463G= MANE Select	NP_940980.4:p.Val1155=