Canonical Allele Identifier: CA2031025709

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363402G= , CM000674.2:g.40363402G=	GRCh38
NC_000012.11:g.40757204G= , CM000674.1:g.40757204G=	GRCh37
NC_000012.10:g.39043471G=	NCBI36
NG_011709.1:g.143392G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029G= MANE Select	ENSP00000298910.7:p.Leu2343=
ENST00000636518.1:c.826G=
ENST00000679360.1:c.*5938G=	ENSP00000505368.1:n.*5938G=
ENST00000679532.1:c.2803G=
ENST00000679683.1:c.819G=
ENST00000680018.1:c.2474G=	ENSP00000505347.1:n.2474G=
ENST00000680422.1:c.4116G=
ENST00000680425.1:c.2196G=	ENSP00000506459.1:n.2196G=
ENST00000680453.1:c.2486G=
ENST00000680790.1:c.6774G=	ENSP00000505335.1:p.Leu2258=
ENST00000681136.1:n.3013G=
ENST00000681696.1:c.2712G=	ENSP00000505871.1:p.Leu904=
ENST00000681773.1:n.236G=
ENST00000298910.11:c.7029G=	ENSP00000298910.7:p.Leu2343=
ENST00000430804.5:c.4325G=
ENST00000479187.5:n.3710G=
NM_198578.3:c.7029G=	NP_940980.3:p.Leu2343=
XM_005268629.2:c.7029G=	XP_005268686.1:p.Leu2343=
XM_011537877.1:c.7029G=	XP_011536179.1:p.Leu2343=
XM_011537879.1:c.5826G=	XP_011536181.1:p.Leu1942=
XR_944868.1:n.485-8575C=
XM_005268629.4:c.7029G=	XP_005268686.1:p.Leu2343=
XM_011537877.3:c.7029G=	XP_011536179.1:p.Leu2343=
XM_017018787.1:c.3945G=	XP_016874276.1:p.Leu1315=
XM_017018788.2:c.3291G=	XP_016874277.1:p.Leu1097=
XM_024448833.1:c.5826G=	XP_024304601.1:p.Leu1942=
XR_944868.2:n.485-8575C=
NM_198578.4:c.7029G= MANE Select	NP_940980.4:p.Leu2343=