Canonical Allele Identifier: CA2031027279

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340404T= , CM000674.2:g.40340404T=	GRCh38
NC_000012.11:g.40734206T= , CM000674.1:g.40734206T=	GRCh37
NC_000012.10:g.39020473T=	NCBI36
NG_011709.1:g.120394T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6059T= MANE Select	ENSP00000298910.7:p.Ile2020=
ENST00000679360.1:c.*4968T=	ENSP00000505368.1:n.*4968T=
ENST00000679532.1:c.1833T=
ENST00000680018.1:c.1504T=	ENSP00000505347.1:n.1504T=
ENST00000680422.1:c.1704T=
ENST00000680425.1:c.1226T=	ENSP00000506459.1:n.1226T=
ENST00000680453.1:c.1516T=
ENST00000680790.1:c.5804T=	ENSP00000505335.1:p.Ile1935=
ENST00000681136.1:n.2043T=
ENST00000681696.1:c.1742T=	ENSP00000505871.1:p.Ile581=
ENST00000298910.11:c.6059T=	ENSP00000298910.7:p.Ile2020=
ENST00000430804.5:c.3355T=
ENST00000479187.5:n.2740T=
NM_198578.3:c.6059T=	NP_940980.3:p.Ile2020=
XM_005268629.2:c.6059T=	XP_005268686.1:p.Ile2020=
XM_011537877.1:c.6059T=	XP_011536179.1:p.Ile2020=
XM_011537878.1:c.6059T=	XP_011536180.1:p.Ile2020=
XM_011537879.1:c.4856T=	XP_011536181.1:p.Ile1619=
XM_005268629.4:c.6059T=	XP_005268686.1:p.Ile2020=
XM_011537877.3:c.6059T=	XP_011536179.1:p.Ile2020=
XM_017018787.1:c.2975T=	XP_016874276.1:p.Ile992=
XM_017018788.2:c.2321T=	XP_016874277.1:p.Ile774=
XM_024448833.1:c.4856T=	XP_024304601.1:p.Ile1619=
NM_198578.4:c.6059T= MANE Select	NP_940980.4:p.Ile2020=