Canonical Allele Identifier: CA384413352

Gene: LRRK2

Linked Data

• dbSNP Id: rs1946779277
• MyVariant Identifiers: chr12:g.40757277C>A (hg19) ; chr12:g.40363475C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363475C>A , CM000674.2:g.40363475C>A	GRCh38
NC_000012.11:g.40757277C>A , CM000674.1:g.40757277C>A	GRCh37
NC_000012.10:g.39043544C>A	NCBI36
NG_011709.1:g.143465C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7102C>A MANE Select	ENSP00000298910.7:p.Gln2368Lys
ENST00000636518.1:c.899C>A
ENST00000679360.1:c.*6011C>A	ENSP00000505368.1:n.*6011C>A
ENST00000679532.1:c.2876C>A
ENST00000679683.1:c.892C>A
ENST00000680018.1:c.2547C>A	ENSP00000505347.1:n.2547C>A
ENST00000680422.1:c.4189C>A
ENST00000680425.1:c.2269C>A	ENSP00000506459.1:n.2269C>A
ENST00000680453.1:c.2559C>A
ENST00000680790.1:c.6847C>A	ENSP00000505335.1:p.Gln2283Lys
ENST00000681136.1:n.3086C>A
ENST00000681696.1:c.2785C>A	ENSP00000505871.1:p.Gln929Lys
ENST00000681773.1:n.309C>A
ENST00000298910.11:c.7102C>A	ENSP00000298910.7:p.Gln2368Lys
ENST00000430804.5:c.4398C>A
ENST00000479187.5:n.3783C>A
NM_198578.3:c.7102C>A	NP_940980.3:p.Gln2368Lys
XM_005268629.2:c.7102C>A	XP_005268686.1:p.Gln2368Lys
XM_011537877.1:c.7102C>A	XP_011536179.1:p.Gln2368Lys
XM_011537879.1:c.5899C>A	XP_011536181.1:p.Gln1967Lys
XR_944868.1:n.485-8648G>T
XM_005268629.4:c.7102C>A	XP_005268686.1:p.Gln2368Lys
XM_011537877.3:c.7102C>A	XP_011536179.1:p.Gln2368Lys
XM_017018787.1:c.4018C>A	XP_016874276.1:p.Gln1340Lys
XM_017018788.2:c.3364C>A	XP_016874277.1:p.Gln1122Lys
XM_024448833.1:c.5899C>A	XP_024304601.1:p.Gln1967Lys
XR_944868.2:n.485-8648G>T
NM_198578.4:c.7102C>A MANE Select	NP_940980.4:p.Gln2368Lys