Canonical Allele Identifier: CA2031025962

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363490G= , CM000674.2:g.40363490G=	GRCh38
NC_000012.11:g.40757292G= , CM000674.1:g.40757292G=	GRCh37
NC_000012.10:g.39043559G=	NCBI36
NG_011709.1:g.143480G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7117G= MANE Select	ENSP00000298910.7:p.Val2373=
ENST00000636518.1:c.914G=
ENST00000679360.1:c.*6026G=	ENSP00000505368.1:n.*6026G=
ENST00000679532.1:c.2891G=
ENST00000679683.1:c.907G=
ENST00000680018.1:c.2562G=	ENSP00000505347.1:n.2562G=
ENST00000680422.1:c.4204G=
ENST00000680425.1:c.2284G=	ENSP00000506459.1:n.2284G=
ENST00000680453.1:c.2574G=
ENST00000680790.1:c.6862G=	ENSP00000505335.1:p.Val2288=
ENST00000681136.1:n.3101G=
ENST00000681696.1:c.2800G=	ENSP00000505871.1:p.Val934=
ENST00000681773.1:n.324G=
ENST00000298910.11:c.7117G=	ENSP00000298910.7:p.Val2373=
ENST00000430804.5:c.4413G=
ENST00000479187.5:n.3798G=
NM_198578.3:c.7117G=	NP_940980.3:p.Val2373=
XM_005268629.2:c.7117G=	XP_005268686.1:p.Val2373=
XM_011537877.1:c.7117G=	XP_011536179.1:p.Val2373=
XM_011537879.1:c.5914G=	XP_011536181.1:p.Val1972=
XR_944868.1:n.485-8663C=
XM_005268629.4:c.7117G=	XP_005268686.1:p.Val2373=
XM_011537877.3:c.7117G=	XP_011536179.1:p.Val2373=
XM_017018787.1:c.4033G=	XP_016874276.1:p.Val1345=
XM_017018788.2:c.3379G=	XP_016874277.1:p.Val1127=
XM_024448833.1:c.5914G=	XP_024304601.1:p.Val1972=
XR_944868.2:n.485-8663C=
NM_198578.4:c.7117G= MANE Select	NP_940980.4:p.Val2373=