Canonical Allele Identifier: CA2031027108

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340295T= , CM000674.2:g.40340295T=	GRCh38
NC_000012.11:g.40734097T= , CM000674.1:g.40734097T=	GRCh37
NC_000012.10:g.39020364T=	NCBI36
NG_011709.1:g.120285T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5950T= MANE Select	ENSP00000298910.7:p.Tyr1984=
ENST00000679360.1:c.*4859T=	ENSP00000505368.1:n.*4859T=
ENST00000679532.1:c.1724T=
ENST00000680018.1:c.1395T=	ENSP00000505347.1:n.1395T=
ENST00000680422.1:c.1595T=
ENST00000680425.1:c.1117T=	ENSP00000506459.1:n.1117T=
ENST00000680453.1:c.1407T=
ENST00000680790.1:c.5695T=	ENSP00000505335.1:p.Tyr1899=
ENST00000681136.1:n.1934T=
ENST00000681696.1:c.1633T=	ENSP00000505871.1:p.Tyr545=
ENST00000298910.11:c.5950T=	ENSP00000298910.7:p.Tyr1984=
ENST00000430804.5:c.3246T=
ENST00000479187.5:n.2631T=
NM_198578.3:c.5950T=	NP_940980.3:p.Tyr1984=
XM_005268629.2:c.5950T=	XP_005268686.1:p.Tyr1984=
XM_011537877.1:c.5950T=	XP_011536179.1:p.Tyr1984=
XM_011537878.1:c.5950T=	XP_011536180.1:p.Tyr1984=
XM_011537879.1:c.4747T=	XP_011536181.1:p.Tyr1583=
XM_005268629.4:c.5950T=	XP_005268686.1:p.Tyr1984=
XM_011537877.3:c.5950T=	XP_011536179.1:p.Tyr1984=
XM_017018787.1:c.2866T=	XP_016874276.1:p.Tyr956=
XM_017018788.2:c.2212T=	XP_016874277.1:p.Tyr738=
XM_024448833.1:c.4747T=	XP_024304601.1:p.Tyr1583=
NM_198578.4:c.5950T= MANE Select	NP_940980.4:p.Tyr1984=