Canonical Allele Identifier: CA2031025970

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363500G= , CM000674.2:g.40363500G=	GRCh38
NC_000012.11:g.40757302G= , CM000674.1:g.40757302G=	GRCh37
NC_000012.10:g.39043569G=	NCBI36
NG_011709.1:g.143490G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7127G= MANE Select	ENSP00000298910.7:p.Trp2376=
ENST00000636518.1:c.924G=
ENST00000679360.1:c.*6036G=	ENSP00000505368.1:n.*6036G=
ENST00000679532.1:c.2901G=
ENST00000679683.1:c.917G=
ENST00000680018.1:c.2572G=	ENSP00000505347.1:n.2572G=
ENST00000680422.1:c.4214G=
ENST00000680425.1:c.2294G=	ENSP00000506459.1:n.2294G=
ENST00000680453.1:c.2584G=
ENST00000680790.1:c.6872G=	ENSP00000505335.1:p.Trp2291=
ENST00000681136.1:n.3111G=
ENST00000681696.1:c.2810G=	ENSP00000505871.1:p.Trp937=
ENST00000681773.1:n.334G=
ENST00000298910.11:c.7127G=	ENSP00000298910.7:p.Trp2376=
ENST00000430804.5:c.4423G=
ENST00000479187.5:n.3808G=
NM_198578.3:c.7127G=	NP_940980.3:p.Trp2376=
XM_005268629.2:c.7127G=	XP_005268686.1:p.Trp2376=
XM_011537877.1:c.7127G=	XP_011536179.1:p.Trp2376=
XM_011537879.1:c.5924G=	XP_011536181.1:p.Trp1975=
XR_944868.1:n.485-8673C=
XM_005268629.4:c.7127G=	XP_005268686.1:p.Trp2376=
XM_011537877.3:c.7127G=	XP_011536179.1:p.Trp2376=
XM_017018787.1:c.4043G=	XP_016874276.1:p.Trp1348=
XM_017018788.2:c.3389G=	XP_016874277.1:p.Trp1130=
XM_024448833.1:c.5924G=	XP_024304601.1:p.Trp1975=
XR_944868.2:n.485-8673C=
NM_198578.4:c.7127G= MANE Select	NP_940980.4:p.Trp2376=