Canonical Allele Identifier: CA384406659

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40745395T>A (hg19) ; chr12:g.40351593T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40351593T>A , CM000674.2:g.40351593T>A	GRCh38
NC_000012.11:g.40745395T>A , CM000674.1:g.40745395T>A	GRCh37
NC_000012.10:g.39031662T>A	NCBI36
NG_011709.1:g.131583T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6436T>A MANE Select	ENSP00000298910.7:p.Leu2146Ile
ENST00000636518.1:c.233T>A
ENST00000679360.1:c.*5345T>A	ENSP00000505368.1:n.*5345T>A
ENST00000679532.1:c.2210T>A
ENST00000679683.1:c.226T>A
ENST00000680018.1:c.1881T>A	ENSP00000505347.1:n.1881T>A
ENST00000680422.1:c.2081T>A
ENST00000680425.1:c.1603T>A	ENSP00000506459.1:n.1603T>A
ENST00000680453.1:c.1893T>A
ENST00000680790.1:c.6181T>A	ENSP00000505335.1:p.Leu2061Ile
ENST00000681136.1:n.2420T>A
ENST00000681696.1:c.2119T>A	ENSP00000505871.1:p.Leu707Ile
ENST00000298910.11:c.6436T>A	ENSP00000298910.7:p.Leu2146Ile
ENST00000430804.5:c.3732T>A
ENST00000479187.5:n.3117T>A
NM_198578.3:c.6436T>A	NP_940980.3:p.Leu2146Ile
XM_005268629.2:c.6436T>A	XP_005268686.1:p.Leu2146Ile
XM_011537877.1:c.6436T>A	XP_011536179.1:p.Leu2146Ile
XM_011537878.1:c.6436T>A	XP_011536180.1:p.Leu2146Ile
XM_011537879.1:c.5233T>A	XP_011536181.1:p.Leu1745Ile
XM_005268629.4:c.6436T>A	XP_005268686.1:p.Leu2146Ile
XM_011537877.3:c.6436T>A	XP_011536179.1:p.Leu2146Ile
XM_017018787.1:c.3352T>A	XP_016874276.1:p.Leu1118Ile
XM_017018788.2:c.2698T>A	XP_016874277.1:p.Leu900Ile
XM_024448833.1:c.5233T>A	XP_024304601.1:p.Leu1745Ile
NM_198578.4:c.6436T>A MANE Select	NP_940980.4:p.Leu2146Ile