Canonical Allele Identifier: CA2031027270

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340400G= , CM000674.2:g.40340400G=	GRCh38
NC_000012.11:g.40734202G= , CM000674.1:g.40734202G=	GRCh37
NC_000012.10:g.39020469G=	NCBI36
NG_011709.1:g.120390G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6055G= MANE Select	ENSP00000298910.7:p.Gly2019=
ENST00000679360.1:c.*4964G=	ENSP00000505368.1:n.*4964G=
ENST00000679532.1:c.1829G=
ENST00000680018.1:c.1500G=	ENSP00000505347.1:n.1500G=
ENST00000680422.1:c.1700G=
ENST00000680425.1:c.1222G=	ENSP00000506459.1:n.1222G=
ENST00000680453.1:c.1512G=
ENST00000680790.1:c.5800G=	ENSP00000505335.1:p.Gly1934=
ENST00000681136.1:n.2039G=
ENST00000681696.1:c.1738G=	ENSP00000505871.1:p.Gly580=
ENST00000298910.11:c.6055G=	ENSP00000298910.7:p.Gly2019=
ENST00000430804.5:c.3351G=
ENST00000479187.5:n.2736G=
NM_198578.3:c.6055G=	NP_940980.3:p.Gly2019=
XM_005268629.2:c.6055G=	XP_005268686.1:p.Gly2019=
XM_011537877.1:c.6055G=	XP_011536179.1:p.Gly2019=
XM_011537878.1:c.6055G=	XP_011536180.1:p.Gly2019=
XM_011537879.1:c.4852G=	XP_011536181.1:p.Gly1618=
XM_005268629.4:c.6055G=	XP_005268686.1:p.Gly2019=
XM_011537877.3:c.6055G=	XP_011536179.1:p.Gly2019=
XM_017018787.1:c.2971G=	XP_016874276.1:p.Gly991=
XM_017018788.2:c.2317G=	XP_016874277.1:p.Gly773=
XM_024448833.1:c.4852G=	XP_024304601.1:p.Gly1618=
NM_198578.4:c.6055G= MANE Select	NP_940980.4:p.Gly2019=