Canonical Allele Identifier: CA2031025767

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363426T= , CM000674.2:g.40363426T=	GRCh38
NC_000012.11:g.40757228T= , CM000674.1:g.40757228T=	GRCh37
NC_000012.10:g.39043495T=	NCBI36
NG_011709.1:g.143416T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7053T= MANE Select	ENSP00000298910.7:p.Asp2351=
ENST00000636518.1:c.850T=
ENST00000679360.1:c.*5962T=	ENSP00000505368.1:n.*5962T=
ENST00000679532.1:c.2827T=
ENST00000679683.1:c.843T=
ENST00000680018.1:c.2498T=	ENSP00000505347.1:n.2498T=
ENST00000680422.1:c.4140T=
ENST00000680425.1:c.2220T=	ENSP00000506459.1:n.2220T=
ENST00000680453.1:c.2510T=
ENST00000680790.1:c.6798T=	ENSP00000505335.1:p.Asp2266=
ENST00000681136.1:n.3037T=
ENST00000681696.1:c.2736T=	ENSP00000505871.1:p.Asp912=
ENST00000681773.1:n.260T=
ENST00000298910.11:c.7053T=	ENSP00000298910.7:p.Asp2351=
ENST00000430804.5:c.4349T=
ENST00000479187.5:n.3734T=
NM_198578.3:c.7053T=	NP_940980.3:p.Asp2351=
XM_005268629.2:c.7053T=	XP_005268686.1:p.Asp2351=
XM_011537877.1:c.7053T=	XP_011536179.1:p.Asp2351=
XM_011537879.1:c.5850T=	XP_011536181.1:p.Asp1950=
XR_944868.1:n.485-8599A=
XM_005268629.4:c.7053T=	XP_005268686.1:p.Asp2351=
XM_011537877.3:c.7053T=	XP_011536179.1:p.Asp2351=
XM_017018787.1:c.3969T=	XP_016874276.1:p.Asp1323=
XM_017018788.2:c.3315T=	XP_016874277.1:p.Asp1105=
XM_024448833.1:c.5850T=	XP_024304601.1:p.Asp1950=
XR_944868.2:n.485-8599A=
NM_198578.4:c.7053T= MANE Select	NP_940980.4:p.Asp2351=