Canonical Allele Identifier: CA384404164

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734244G>C (hg19) ; chr12:g.40340442G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340442G>C , CM000674.2:g.40340442G>C	GRCh38
NC_000012.11:g.40734244G>C , CM000674.1:g.40734244G>C	GRCh37
NC_000012.10:g.39020511G>C	NCBI36
NG_011709.1:g.120432G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6097G>C MANE Select	ENSP00000298910.7:p.Glu2033Gln
ENST00000679360.1:c.*5006G>C	ENSP00000505368.1:n.*5006G>C
ENST00000679532.1:c.1871G>C
ENST00000680018.1:c.1542G>C	ENSP00000505347.1:n.1542G>C
ENST00000680422.1:c.1742G>C
ENST00000680425.1:c.1264G>C	ENSP00000506459.1:n.1264G>C
ENST00000680453.1:c.1554G>C
ENST00000680790.1:c.5842G>C	ENSP00000505335.1:p.Glu1948Gln
ENST00000681136.1:n.2081G>C
ENST00000681696.1:c.1780G>C	ENSP00000505871.1:p.Glu594Gln
ENST00000298910.11:c.6097G>C	ENSP00000298910.7:p.Glu2033Gln
ENST00000430804.5:c.3393G>C
ENST00000479187.5:n.2778G>C
NM_198578.3:c.6097G>C	NP_940980.3:p.Glu2033Gln
XM_005268629.2:c.6097G>C	XP_005268686.1:p.Glu2033Gln
XM_011537877.1:c.6097G>C	XP_011536179.1:p.Glu2033Gln
XM_011537878.1:c.6097G>C	XP_011536180.1:p.Glu2033Gln
XM_011537879.1:c.4894G>C	XP_011536181.1:p.Glu1632Gln
XM_005268629.4:c.6097G>C	XP_005268686.1:p.Glu2033Gln
XM_011537877.3:c.6097G>C	XP_011536179.1:p.Glu2033Gln
XM_017018787.1:c.3013G>C	XP_016874276.1:p.Glu1005Gln
XM_017018788.2:c.2359G>C	XP_016874277.1:p.Glu787Gln
XM_024448833.1:c.4894G>C	XP_024304601.1:p.Glu1632Gln
NM_198578.4:c.6097G>C MANE Select	NP_940980.4:p.Glu2033Gln