Canonical Allele Identifier: CA2031025723

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363409T= , CM000674.2:g.40363409T=	GRCh38
NC_000012.11:g.40757211T= , CM000674.1:g.40757211T=	GRCh37
NC_000012.10:g.39043478T=	NCBI36
NG_011709.1:g.143399T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7036T= MANE Select	ENSP00000298910.7:p.Tyr2346=
ENST00000636518.1:c.833T=
ENST00000679360.1:c.*5945T=	ENSP00000505368.1:n.*5945T=
ENST00000679532.1:c.2810T=
ENST00000679683.1:c.826T=
ENST00000680018.1:c.2481T=	ENSP00000505347.1:n.2481T=
ENST00000680422.1:c.4123T=
ENST00000680425.1:c.2203T=	ENSP00000506459.1:n.2203T=
ENST00000680453.1:c.2493T=
ENST00000680790.1:c.6781T=	ENSP00000505335.1:p.Tyr2261=
ENST00000681136.1:n.3020T=
ENST00000681696.1:c.2719T=	ENSP00000505871.1:p.Tyr907=
ENST00000681773.1:n.243T=
ENST00000298910.11:c.7036T=	ENSP00000298910.7:p.Tyr2346=
ENST00000430804.5:c.4332T=
ENST00000479187.5:n.3717T=
NM_198578.3:c.7036T=	NP_940980.3:p.Tyr2346=
XM_005268629.2:c.7036T=	XP_005268686.1:p.Tyr2346=
XM_011537877.1:c.7036T=	XP_011536179.1:p.Tyr2346=
XM_011537879.1:c.5833T=	XP_011536181.1:p.Tyr1945=
XR_944868.1:n.485-8582A=
XM_005268629.4:c.7036T=	XP_005268686.1:p.Tyr2346=
XM_011537877.3:c.7036T=	XP_011536179.1:p.Tyr2346=
XM_017018787.1:c.3952T=	XP_016874276.1:p.Tyr1318=
XM_017018788.2:c.3298T=	XP_016874277.1:p.Tyr1100=
XM_024448833.1:c.5833T=	XP_024304601.1:p.Tyr1945=
XR_944868.2:n.485-8582A=
NM_198578.4:c.7036T= MANE Select	NP_940980.4:p.Tyr2346=