Canonical Allele Identifier: CA2031025738

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363411T= , CM000674.2:g.40363411T=	GRCh38
NC_000012.11:g.40757213T= , CM000674.1:g.40757213T=	GRCh37
NC_000012.10:g.39043480T=	NCBI36
NG_011709.1:g.143401T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7038T= MANE Select	ENSP00000298910.7:p.Tyr2346=
ENST00000636518.1:c.835T=
ENST00000679360.1:c.*5947T=	ENSP00000505368.1:n.*5947T=
ENST00000679532.1:c.2812T=
ENST00000679683.1:c.828T=
ENST00000680018.1:c.2483T=	ENSP00000505347.1:n.2483T=
ENST00000680422.1:c.4125T=
ENST00000680425.1:c.2205T=	ENSP00000506459.1:n.2205T=
ENST00000680453.1:c.2495T=
ENST00000680790.1:c.6783T=	ENSP00000505335.1:p.Tyr2261=
ENST00000681136.1:n.3022T=
ENST00000681696.1:c.2721T=	ENSP00000505871.1:p.Tyr907=
ENST00000681773.1:n.245T=
ENST00000298910.11:c.7038T=	ENSP00000298910.7:p.Tyr2346=
ENST00000430804.5:c.4334T=
ENST00000479187.5:n.3719T=
NM_198578.3:c.7038T=	NP_940980.3:p.Tyr2346=
XM_005268629.2:c.7038T=	XP_005268686.1:p.Tyr2346=
XM_011537877.1:c.7038T=	XP_011536179.1:p.Tyr2346=
XM_011537879.1:c.5835T=	XP_011536181.1:p.Tyr1945=
XR_944868.1:n.485-8584A=
XM_005268629.4:c.7038T=	XP_005268686.1:p.Tyr2346=
XM_011537877.3:c.7038T=	XP_011536179.1:p.Tyr2346=
XM_017018787.1:c.3954T=	XP_016874276.1:p.Tyr1318=
XM_017018788.2:c.3300T=	XP_016874277.1:p.Tyr1100=
XM_024448833.1:c.5835T=	XP_024304601.1:p.Tyr1945=
XR_944868.2:n.485-8584A=
NM_198578.4:c.7038T= MANE Select	NP_940980.4:p.Tyr2346=