Canonical Allele Identifier: CA2031025729

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363410A= , CM000674.2:g.40363410A=	GRCh38
NC_000012.11:g.40757212A= , CM000674.1:g.40757212A=	GRCh37
NC_000012.10:g.39043479A=	NCBI36
NG_011709.1:g.143400A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7037A= MANE Select	ENSP00000298910.7:p.Tyr2346=
ENST00000636518.1:c.834A=
ENST00000679360.1:c.*5946A=	ENSP00000505368.1:n.*5946A=
ENST00000679532.1:c.2811A=
ENST00000679683.1:c.827A=
ENST00000680018.1:c.2482A=	ENSP00000505347.1:n.2482A=
ENST00000680422.1:c.4124A=
ENST00000680425.1:c.2204A=	ENSP00000506459.1:n.2204A=
ENST00000680453.1:c.2494A=
ENST00000680790.1:c.6782A=	ENSP00000505335.1:p.Tyr2261=
ENST00000681136.1:n.3021A=
ENST00000681696.1:c.2720A=	ENSP00000505871.1:p.Tyr907=
ENST00000681773.1:n.244A=
ENST00000298910.11:c.7037A=	ENSP00000298910.7:p.Tyr2346=
ENST00000430804.5:c.4333A=
ENST00000479187.5:n.3718A=
NM_198578.3:c.7037A=	NP_940980.3:p.Tyr2346=
XM_005268629.2:c.7037A=	XP_005268686.1:p.Tyr2346=
XM_011537877.1:c.7037A=	XP_011536179.1:p.Tyr2346=
XM_011537879.1:c.5834A=	XP_011536181.1:p.Tyr1945=
XR_944868.1:n.485-8583T=
XM_005268629.4:c.7037A=	XP_005268686.1:p.Tyr2346=
XM_011537877.3:c.7037A=	XP_011536179.1:p.Tyr2346=
XM_017018787.1:c.3953A=	XP_016874276.1:p.Tyr1318=
XM_017018788.2:c.3299A=	XP_016874277.1:p.Tyr1100=
XM_024448833.1:c.5834A=	XP_024304601.1:p.Tyr1945=
XR_944868.2:n.485-8583T=
NM_198578.4:c.7037A= MANE Select	NP_940980.4:p.Tyr2346=