Canonical Allele Identifier: CA2031027272

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340401G= , CM000674.2:g.40340401G=	GRCh38
NC_000012.11:g.40734203G= , CM000674.1:g.40734203G=	GRCh37
NC_000012.10:g.39020470G=	NCBI36
NG_011709.1:g.120391G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6056G= MANE Select	ENSP00000298910.7:p.Gly2019=
ENST00000679360.1:c.*4965G=	ENSP00000505368.1:n.*4965G=
ENST00000679532.1:c.1830G=
ENST00000680018.1:c.1501G=	ENSP00000505347.1:n.1501G=
ENST00000680422.1:c.1701G=
ENST00000680425.1:c.1223G=	ENSP00000506459.1:n.1223G=
ENST00000680453.1:c.1513G=
ENST00000680790.1:c.5801G=	ENSP00000505335.1:p.Gly1934=
ENST00000681136.1:n.2040G=
ENST00000681696.1:c.1739G=	ENSP00000505871.1:p.Gly580=
ENST00000298910.11:c.6056G=	ENSP00000298910.7:p.Gly2019=
ENST00000430804.5:c.3352G=
ENST00000479187.5:n.2737G=
NM_198578.3:c.6056G=	NP_940980.3:p.Gly2019=
XM_005268629.2:c.6056G=	XP_005268686.1:p.Gly2019=
XM_011537877.1:c.6056G=	XP_011536179.1:p.Gly2019=
XM_011537878.1:c.6056G=	XP_011536180.1:p.Gly2019=
XM_011537879.1:c.4853G=	XP_011536181.1:p.Gly1618=
XM_005268629.4:c.6056G=	XP_005268686.1:p.Gly2019=
XM_011537877.3:c.6056G=	XP_011536179.1:p.Gly2019=
XM_017018787.1:c.2972G=	XP_016874276.1:p.Gly991=
XM_017018788.2:c.2318G=	XP_016874277.1:p.Gly773=
XM_024448833.1:c.4853G=	XP_024304601.1:p.Gly1618=
NM_198578.4:c.6056G= MANE Select	NP_940980.4:p.Gly2019=