Canonical Allele Identifier: CA2031025880

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363460C= , CM000674.2:g.40363460C=	GRCh38
NC_000012.11:g.40757262C= , CM000674.1:g.40757262C=	GRCh37
NC_000012.10:g.39043529C=	NCBI36
NG_011709.1:g.143450C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7087C= MANE Select	ENSP00000298910.7:p.Leu2363=
ENST00000636518.1:c.884C=
ENST00000679360.1:c.*5996C=	ENSP00000505368.1:n.*5996C=
ENST00000679532.1:c.2861C=
ENST00000679683.1:c.877C=
ENST00000680018.1:c.2532C=	ENSP00000505347.1:n.2532C=
ENST00000680422.1:c.4174C=
ENST00000680425.1:c.2254C=	ENSP00000506459.1:n.2254C=
ENST00000680453.1:c.2544C=
ENST00000680790.1:c.6832C=	ENSP00000505335.1:p.Leu2278=
ENST00000681136.1:n.3071C=
ENST00000681696.1:c.2770C=	ENSP00000505871.1:p.Leu924=
ENST00000681773.1:n.294C=
ENST00000298910.11:c.7087C=	ENSP00000298910.7:p.Leu2363=
ENST00000430804.5:c.4383C=
ENST00000479187.5:n.3768C=
NM_198578.3:c.7087C=	NP_940980.3:p.Leu2363=
XM_005268629.2:c.7087C=	XP_005268686.1:p.Leu2363=
XM_011537877.1:c.7087C=	XP_011536179.1:p.Leu2363=
XM_011537879.1:c.5884C=	XP_011536181.1:p.Leu1962=
XR_944868.1:n.485-8633G=
XM_005268629.4:c.7087C=	XP_005268686.1:p.Leu2363=
XM_011537877.3:c.7087C=	XP_011536179.1:p.Leu2363=
XM_017018787.1:c.4003C=	XP_016874276.1:p.Leu1335=
XM_017018788.2:c.3349C=	XP_016874277.1:p.Leu1117=
XM_024448833.1:c.5884C=	XP_024304601.1:p.Leu1962=
XR_944868.2:n.485-8633G=
NM_198578.4:c.7087C= MANE Select	NP_940980.4:p.Leu2363=