Canonical Allele Identifier: CA2030994987

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320095C= , CM000674.2:g.40320095C=	GRCh38
NC_000012.11:g.40713897C= , CM000674.1:g.40713897C=	GRCh37
NC_000012.10:g.39000164C=	NCBI36
NG_011709.1:g.100085C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4935C= MANE Select	ENSP00000298910.7:p.Tyr1645=
ENST00000679360.1:c.*3844C=	ENSP00000505368.1:n.*3844C=
ENST00000679532.1:c.709C=
ENST00000680018.1:c.380C=	ENSP00000505347.1:n.380C=
ENST00000680422.1:c.580C=
ENST00000680425.1:c.183-939C=	ENSP00000506459.1:n.183-939C=
ENST00000680453.1:c.473-939C=
ENST00000680790.1:c.4680C=	ENSP00000505335.1:p.Tyr1560=
ENST00000681136.1:n.919C=
ENST00000681696.1:c.618C=	ENSP00000505871.1:p.Tyr206=
ENST00000298910.11:c.4935C=	ENSP00000298910.7:p.Tyr1645=
ENST00000430804.5:c.2231C=
ENST00000479187.5:n.1616C=
NM_198578.3:c.4935C=	NP_940980.3:p.Tyr1645=
XM_005268629.2:c.4935C=	XP_005268686.1:p.Tyr1645=
XM_011537877.1:c.4935C=	XP_011536179.1:p.Tyr1645=
XM_011537878.1:c.4935C=	XP_011536180.1:p.Tyr1645=
XM_011537879.1:c.3732C=	XP_011536181.1:p.Tyr1244=
XM_011537881.1:c.4828-939C=	XP_011536183.1:n.4828-939C=
XM_005268629.4:c.4935C=	XP_005268686.1:p.Tyr1645=
XM_011537877.3:c.4935C=	XP_011536179.1:p.Tyr1645=
XM_011537881.3:c.4828-939C=	XP_011536183.1:n.4828-939C=
XM_017018787.1:c.1851C=	XP_016874276.1:p.Tyr617=
XM_017018788.2:c.1197C=	XP_016874277.1:p.Tyr399=
XM_024448833.1:c.3732C=	XP_024304601.1:p.Tyr1244=
XR_001748574.2:n.5303C=
NM_198578.4:c.4935C= MANE Select	NP_940980.4:p.Tyr1645=