Canonical Allele Identifier: CA2031026151

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363582C= , CM000674.2:g.40363582C=	GRCh38
NC_000012.11:g.40757384C= , CM000674.1:g.40757384C=	GRCh37
NC_000012.10:g.39043651C=	NCBI36
NG_011709.1:g.143572C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7181+28C= MANE Select	ENSP00000298910.7:n.7181+28C=
ENST00000636518.1:c.978+28C=
ENST00000679360.1:c.*6090+28C=	ENSP00000505368.1:n.*6090+28C=
ENST00000679532.1:c.2955+28C=
ENST00000679683.1:c.971+28C=
ENST00000680018.1:c.2626+28C=	ENSP00000505347.1:n.2626+28C=
ENST00000680422.1:c.4268+28C=
ENST00000680425.1:c.2348+28C=	ENSP00000506459.1:n.2348+28C=
ENST00000680453.1:c.2638+28C=
ENST00000680790.1:c.6926+28C=	ENSP00000505335.1:n.6926+28C=
ENST00000681136.1:n.3165+28C=
ENST00000681696.1:c.2864+28C=	ENSP00000505871.1:n.2864+28C=
ENST00000681773.1:n.388+28C=
ENST00000298910.11:c.7181+28C=	ENSP00000298910.7:n.7181+28C=
ENST00000430804.5:c.4477+28C=
ENST00000479187.5:n.3862+28C=
NM_198578.3:c.7181+28C=	NP_940980.3:n.7181+28C=
XM_005268629.2:c.7181+28C=	XP_005268686.1:n.7181+28C=
XM_011537877.1:c.7181+28C=	XP_011536179.1:n.7181+28C=
XM_011537879.1:c.5978+28C=	XP_011536181.1:n.5978+28C=
XR_944868.1:n.485-8755G=
XM_005268629.4:c.7181+28C=	XP_005268686.1:n.7181+28C=
XM_011537877.3:c.7181+28C=	XP_011536179.1:n.7181+28C=
XM_017018787.1:c.4097+28C=	XP_016874276.1:n.4097+28C=
XM_017018788.2:c.3443+28C=	XP_016874277.1:n.3443+28C=
XM_024448833.1:c.5978+28C=	XP_024304601.1:n.5978+28C=
XR_944868.2:n.485-8755G=
NM_198578.4:c.7181+28C= MANE Select	NP_940980.4:n.7181+28C=