Canonical Allele Identifier: CA2031026030

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363528A= , CM000674.2:g.40363528A=	GRCh38
NC_000012.11:g.40757330A= , CM000674.1:g.40757330A=	GRCh37
NC_000012.10:g.39043597A=	NCBI36
NG_011709.1:g.143518A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7155A= MANE Select	ENSP00000298910.7:p.Gly2385=
ENST00000636518.1:c.952A=
ENST00000679360.1:c.*6064A=	ENSP00000505368.1:n.*6064A=
ENST00000679532.1:c.2929A=
ENST00000679683.1:c.945A=
ENST00000680018.1:c.2600A=	ENSP00000505347.1:n.2600A=
ENST00000680422.1:c.4242A=
ENST00000680425.1:c.2322A=	ENSP00000506459.1:n.2322A=
ENST00000680453.1:c.2612A=
ENST00000680790.1:c.6900A=	ENSP00000505335.1:p.Gly2300=
ENST00000681136.1:n.3139A=
ENST00000681696.1:c.2838A=	ENSP00000505871.1:p.Gly946=
ENST00000681773.1:n.362A=
ENST00000298910.11:c.7155A=	ENSP00000298910.7:p.Gly2385=
ENST00000430804.5:c.4451A=
ENST00000479187.5:n.3836A=
NM_198578.3:c.7155A=	NP_940980.3:p.Gly2385=
XM_005268629.2:c.7155A=	XP_005268686.1:p.Gly2385=
XM_011537877.1:c.7155A=	XP_011536179.1:p.Gly2385=
XM_011537879.1:c.5952A=	XP_011536181.1:p.Gly1984=
XR_944868.1:n.485-8701T=
XM_005268629.4:c.7155A=	XP_005268686.1:p.Gly2385=
XM_011537877.3:c.7155A=	XP_011536179.1:p.Gly2385=
XM_017018787.1:c.4071A=	XP_016874276.1:p.Gly1357=
XM_017018788.2:c.3417A=	XP_016874277.1:p.Gly1139=
XM_024448833.1:c.5952A=	XP_024304601.1:p.Gly1984=
XR_944868.2:n.485-8701T=
NM_198578.4:c.7155A= MANE Select	NP_940980.4:p.Gly2385=