Canonical Allele Identifier: CA2031000555

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351682C= , CM000674.2:g.40351682C=	GRCh38
NC_000012.11:g.40745484C= , CM000674.1:g.40745484C=	GRCh37
NC_000012.10:g.39031751C=	NCBI36
NG_011709.1:g.131672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6525C= MANE Select	ENSP00000298910.7:p.Asp2175=
ENST00000636518.1:c.322C=
ENST00000679360.1:c.*5434C=	ENSP00000505368.1:n.*5434C=
ENST00000679532.1:c.2299C=
ENST00000679683.1:c.315C=
ENST00000680018.1:c.1970C=	ENSP00000505347.1:n.1970C=
ENST00000680422.1:c.2170C=
ENST00000680425.1:c.1692C=	ENSP00000506459.1:n.1692C=
ENST00000680453.1:c.1982C=
ENST00000680790.1:c.6270C=	ENSP00000505335.1:p.Asp2090=
ENST00000681136.1:n.2509C=
ENST00000681696.1:c.2208C=	ENSP00000505871.1:p.Asp736=
ENST00000298910.11:c.6525C=	ENSP00000298910.7:p.Asp2175=
ENST00000430804.5:c.3821C=
ENST00000479187.5:n.3206C=
NM_198578.3:c.6525C=	NP_940980.3:p.Asp2175=
XM_005268629.2:c.6525C=	XP_005268686.1:p.Asp2175=
XM_011537877.1:c.6525C=	XP_011536179.1:p.Asp2175=
XM_011537878.1:c.6525C=	XP_011536180.1:p.Asp2175=
XM_011537879.1:c.5322C=	XP_011536181.1:p.Asp1774=
XM_005268629.4:c.6525C=	XP_005268686.1:p.Asp2175=
XM_011537877.3:c.6525C=	XP_011536179.1:p.Asp2175=
XM_017018787.1:c.3441C=	XP_016874276.1:p.Asp1147=
XM_017018788.2:c.2787C=	XP_016874277.1:p.Asp929=
XM_024448833.1:c.5322C=	XP_024304601.1:p.Asp1774=
NM_198578.4:c.6525C= MANE Select	NP_940980.4:p.Asp2175=