Canonical Allele Identifier: CA343686

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40364850T= , CM000674.2:g.40364850T=	GRCh38
NC_000012.11:g.40758652T= , CM000674.1:g.40758652T=	GRCh37
NC_000012.10:g.39044919T=	NCBI36
NG_011709.1:g.144840T=

Transcript Alleles

HGVS	Amino-acid Change
NM_198578.4:c.7190T= MANE Select	NP_940980.4:p.Met2397=
ENST00000298910.12:c.7190T= MANE Select	ENSP00000298910.7:p.Met2397=
NM_198578.3:c.7190T=	NP_940980.3:p.Met2397=
ENST00000298910.11:c.7190T=	ENSP00000298910.7:p.Met2397=
ENST00000430804.5:c.4486T=
ENST00000479187.5:n.3871T=
ENST00000636518.1:c.987T=
ENST00000679360.1:c.*6099T=	ENSP00000505368.1:n.*6099T=
ENST00000679532.1:c.2964T=
ENST00000679683.1:c.980T=
ENST00000680018.1:c.2635T=	ENSP00000505347.1:n.2635T=
ENST00000680422.1:c.4277T=
ENST00000680425.1:c.2357T=	ENSP00000506459.1:n.2357T=
ENST00000680453.1:c.2647T=
ENST00000680790.1:c.6935T=	ENSP00000505335.1:p.Met2312=
ENST00000681136.1:n.3174T=
ENST00000681696.1:c.2873T=	ENSP00000505871.1:p.Met958=
ENST00000681773.1:n.397T=
XM_005268629.2:c.7190T=	XP_005268686.1:p.Met2397=
XM_005268629.4:c.7190T=	XP_005268686.1:p.Met2397=
XM_011537877.1:c.7190T=	XP_011536179.1:p.Met2397=
XM_011537877.3:c.7190T=	XP_011536179.1:p.Met2397=
XM_011537879.1:c.5987T=	XP_011536181.1:p.Met1996=
XM_017018787.1:c.4106T=	XP_016874276.1:p.Met1369=
XM_017018788.2:c.3452T=	XP_016874277.1:p.Met1151=
XM_024448833.1:c.5987T=	XP_024304601.1:p.Met1996=
XR_944868.1:n.485-10023A=
XR_944868.2:n.485-10023A=