Canonical Allele Identifier: CA2031026008

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363520C= , CM000674.2:g.40363520C=	GRCh38
NC_000012.11:g.40757322C= , CM000674.1:g.40757322C=	GRCh37
NC_000012.10:g.39043589C=	NCBI36
NG_011709.1:g.143510C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7147C= MANE Select	ENSP00000298910.7:p.Leu2383=
ENST00000636518.1:c.944C=
ENST00000679360.1:c.*6056C=	ENSP00000505368.1:n.*6056C=
ENST00000679532.1:c.2921C=
ENST00000679683.1:c.937C=
ENST00000680018.1:c.2592C=	ENSP00000505347.1:n.2592C=
ENST00000680422.1:c.4234C=
ENST00000680425.1:c.2314C=	ENSP00000506459.1:n.2314C=
ENST00000680453.1:c.2604C=
ENST00000680790.1:c.6892C=	ENSP00000505335.1:p.Leu2298=
ENST00000681136.1:n.3131C=
ENST00000681696.1:c.2830C=	ENSP00000505871.1:p.Leu944=
ENST00000681773.1:n.354C=
ENST00000298910.11:c.7147C=	ENSP00000298910.7:p.Leu2383=
ENST00000430804.5:c.4443C=
ENST00000479187.5:n.3828C=
NM_198578.3:c.7147C=	NP_940980.3:p.Leu2383=
XM_005268629.2:c.7147C=	XP_005268686.1:p.Leu2383=
XM_011537877.1:c.7147C=	XP_011536179.1:p.Leu2383=
XM_011537879.1:c.5944C=	XP_011536181.1:p.Leu1982=
XR_944868.1:n.485-8693G=
XM_005268629.4:c.7147C=	XP_005268686.1:p.Leu2383=
XM_011537877.3:c.7147C=	XP_011536179.1:p.Leu2383=
XM_017018787.1:c.4063C=	XP_016874276.1:p.Leu1355=
XM_017018788.2:c.3409C=	XP_016874277.1:p.Leu1137=
XM_024448833.1:c.5944C=	XP_024304601.1:p.Leu1982=
XR_944868.2:n.485-8693G=
NM_198578.4:c.7147C= MANE Select	NP_940980.4:p.Leu2383=