Canonical Allele Identifier: CA384419730

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713949G>C (hg19) ; chr12:g.40320147G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320147G>C , CM000674.2:g.40320147G>C	GRCh38
NC_000012.11:g.40713949G>C , CM000674.1:g.40713949G>C	GRCh37
NC_000012.10:g.39000216G>C	NCBI36
NG_011709.1:g.100137G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4987G>C MANE Select	ENSP00000298910.7:p.Gly1663Arg
ENST00000679360.1:c.*3896G>C	ENSP00000505368.1:n.*3896G>C
ENST00000679532.1:c.761G>C
ENST00000680018.1:c.432G>C	ENSP00000505347.1:n.432G>C
ENST00000680422.1:c.632G>C
ENST00000680425.1:c.183-887G>C	ENSP00000506459.1:n.183-887G>C
ENST00000680453.1:c.473-887G>C
ENST00000680790.1:c.4732G>C	ENSP00000505335.1:p.Gly1578Arg
ENST00000681136.1:n.971G>C
ENST00000681696.1:c.670G>C	ENSP00000505871.1:p.Gly224Arg
ENST00000298910.11:c.4987G>C	ENSP00000298910.7:p.Gly1663Arg
ENST00000430804.5:c.2283G>C
ENST00000479187.5:n.1668G>C
NM_198578.3:c.4987G>C	NP_940980.3:p.Gly1663Arg
XM_005268629.2:c.4987G>C	XP_005268686.1:p.Gly1663Arg
XM_011537877.1:c.4987G>C	XP_011536179.1:p.Gly1663Arg
XM_011537878.1:c.4987G>C	XP_011536180.1:p.Gly1663Arg
XM_011537879.1:c.3784G>C	XP_011536181.1:p.Gly1262Arg
XM_011537881.1:c.4828-887G>C	XP_011536183.1:n.4828-887G>C
XM_005268629.4:c.4987G>C	XP_005268686.1:p.Gly1663Arg
XM_011537877.3:c.4987G>C	XP_011536179.1:p.Gly1663Arg
XM_011537881.3:c.4828-887G>C	XP_011536183.1:n.4828-887G>C
XM_017018787.1:c.1903G>C	XP_016874276.1:p.Gly635Arg
XM_017018788.2:c.1249G>C	XP_016874277.1:p.Gly417Arg
XM_024448833.1:c.3784G>C	XP_024304601.1:p.Gly1262Arg
XR_001748574.2:n.5355G>C
NM_198578.4:c.4987G>C MANE Select	NP_940980.4:p.Gly1663Arg