Canonical Allele Identifier: CA479268603

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713942G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320140G>A , CM000674.2:g.40320140G>A	GRCh38
NC_000012.11:g.40713942G>A , CM000674.1:g.40713942G>A	GRCh37
NC_000012.10:g.39000209G>A	NCBI36
NG_011709.1:g.100130G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4980G>A MANE Select	ENSP00000298910.7:p.Leu1660=
ENST00000679360.1:c.*3889G>A	ENSP00000505368.1:n.*3889G>A
ENST00000679532.1:c.754G>A
ENST00000680018.1:c.425G>A	ENSP00000505347.1:n.425G>A
ENST00000680422.1:c.625G>A
ENST00000680425.1:c.183-894G>A	ENSP00000506459.1:n.183-894G>A
ENST00000680453.1:c.473-894G>A
ENST00000680790.1:c.4725G>A	ENSP00000505335.1:p.Leu1575=
ENST00000681136.1:n.964G>A
ENST00000681696.1:c.663G>A	ENSP00000505871.1:p.Leu221=
ENST00000298910.11:c.4980G>A	ENSP00000298910.7:p.Leu1660=
ENST00000430804.5:c.2276G>A
ENST00000479187.5:n.1661G>A
NM_198578.3:c.4980G>A	NP_940980.3:p.Leu1660=
XM_005268629.2:c.4980G>A	XP_005268686.1:p.Leu1660=
XM_011537877.1:c.4980G>A	XP_011536179.1:p.Leu1660=
XM_011537878.1:c.4980G>A	XP_011536180.1:p.Leu1660=
XM_011537879.1:c.3777G>A	XP_011536181.1:p.Leu1259=
XM_011537881.1:c.4828-894G>A	XP_011536183.1:n.4828-894G>A
XM_005268629.4:c.4980G>A	XP_005268686.1:p.Leu1660=
XM_011537877.3:c.4980G>A	XP_011536179.1:p.Leu1660=
XM_011537881.3:c.4828-894G>A	XP_011536183.1:n.4828-894G>A
XM_017018787.1:c.1896G>A	XP_016874276.1:p.Leu632=
XM_017018788.2:c.1242G>A	XP_016874277.1:p.Leu414=
XM_024448833.1:c.3777G>A	XP_024304601.1:p.Leu1259=
XR_001748574.2:n.5348G>A
NM_198578.4:c.4980G>A MANE Select	NP_940980.4:p.Leu1660=