Canonical Allele Identifier: CA2031027288

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340411G= , CM000674.2:g.40340411G=	GRCh38
NC_000012.11:g.40734213G= , CM000674.1:g.40734213G=	GRCh37
NC_000012.10:g.39020480G=	NCBI36
NG_011709.1:g.120401G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6066G= MANE Select	ENSP00000298910.7:p.Gln2022=
ENST00000679360.1:c.*4975G=	ENSP00000505368.1:n.*4975G=
ENST00000679532.1:c.1840G=
ENST00000680018.1:c.1511G=	ENSP00000505347.1:n.1511G=
ENST00000680422.1:c.1711G=
ENST00000680425.1:c.1233G=	ENSP00000506459.1:n.1233G=
ENST00000680453.1:c.1523G=
ENST00000680790.1:c.5811G=	ENSP00000505335.1:p.Gln1937=
ENST00000681136.1:n.2050G=
ENST00000681696.1:c.1749G=	ENSP00000505871.1:p.Gln583=
ENST00000298910.11:c.6066G=	ENSP00000298910.7:p.Gln2022=
ENST00000430804.5:c.3362G=
ENST00000479187.5:n.2747G=
NM_198578.3:c.6066G=	NP_940980.3:p.Gln2022=
XM_005268629.2:c.6066G=	XP_005268686.1:p.Gln2022=
XM_011537877.1:c.6066G=	XP_011536179.1:p.Gln2022=
XM_011537878.1:c.6066G=	XP_011536180.1:p.Gln2022=
XM_011537879.1:c.4863G=	XP_011536181.1:p.Gln1621=
XM_005268629.4:c.6066G=	XP_005268686.1:p.Gln2022=
XM_011537877.3:c.6066G=	XP_011536179.1:p.Gln2022=
XM_017018787.1:c.2982G=	XP_016874276.1:p.Gln994=
XM_017018788.2:c.2328G=	XP_016874277.1:p.Gln776=
XM_024448833.1:c.4863G=	XP_024304601.1:p.Gln1621=
NM_198578.4:c.6066G= MANE Select	NP_940980.4:p.Gln2022=