Canonical Allele Identifier: CA384419538

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713862T>A (hg19) ; chr12:g.40320060T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320060T>A , CM000674.2:g.40320060T>A	GRCh38
NC_000012.11:g.40713862T>A , CM000674.1:g.40713862T>A	GRCh37
NC_000012.10:g.39000129T>A	NCBI36
NG_011709.1:g.100050T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4900T>A MANE Select	ENSP00000298910.7:p.Phe1634Ile
ENST00000679360.1:c.*3809T>A	ENSP00000505368.1:n.*3809T>A
ENST00000679532.1:c.674T>A
ENST00000680018.1:c.345T>A	ENSP00000505347.1:n.345T>A
ENST00000680422.1:c.545T>A
ENST00000680425.1:c.183-974T>A	ENSP00000506459.1:n.183-974T>A
ENST00000680453.1:c.473-974T>A
ENST00000680790.1:c.4645T>A	ENSP00000505335.1:p.Phe1549Ile
ENST00000681136.1:n.884T>A
ENST00000681696.1:c.583T>A	ENSP00000505871.1:p.Phe195Ile
ENST00000298910.11:c.4900T>A	ENSP00000298910.7:p.Phe1634Ile
ENST00000430804.5:c.2196T>A
ENST00000479187.5:n.1581T>A
ENST00000481256.1:n.559T>A
NM_198578.3:c.4900T>A	NP_940980.3:p.Phe1634Ile
XM_005268629.2:c.4900T>A	XP_005268686.1:p.Phe1634Ile
XM_011537877.1:c.4900T>A	XP_011536179.1:p.Phe1634Ile
XM_011537878.1:c.4900T>A	XP_011536180.1:p.Phe1634Ile
XM_011537879.1:c.3697T>A	XP_011536181.1:p.Phe1233Ile
XM_011537881.1:c.4828-974T>A	XP_011536183.1:n.4828-974T>A
XM_005268629.4:c.4900T>A	XP_005268686.1:p.Phe1634Ile
XM_011537877.3:c.4900T>A	XP_011536179.1:p.Phe1634Ile
XM_011537881.3:c.4828-974T>A	XP_011536183.1:n.4828-974T>A
XM_017018787.1:c.1816T>A	XP_016874276.1:p.Phe606Ile
XM_017018788.2:c.1162T>A	XP_016874277.1:p.Phe388Ile
XM_024448833.1:c.3697T>A	XP_024304601.1:p.Phe1233Ile
XR_001748574.2:n.5268T>A
NM_198578.4:c.4900T>A MANE Select	NP_940980.4:p.Phe1634Ile