Canonical Allele Identifier: CA384420988

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40716982G>A (hg19) ; chr12:g.40323180G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40323180G>A , CM000674.2:g.40323180G>A	GRCh38
NC_000012.11:g.40716982G>A , CM000674.1:g.40716982G>A	GRCh37
NC_000012.10:g.39003249G>A	NCBI36
NG_011709.1:g.103170G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.5530G>A MANE Select	ENSP00000298910.7:p.Asp1844Asn
ENST00000679360.1:c.*4439G>A	ENSP00000505368.1:n.*4439G>A
ENST00000679532.1:c.1304G>A
ENST00000680018.1:c.975G>A	ENSP00000505347.1:n.975G>A
ENST00000680422.1:c.1175G>A
ENST00000680425.1:c.697G>A	ENSP00000506459.1:n.697G>A
ENST00000680453.1:c.987G>A
ENST00000680790.1:c.5275G>A	ENSP00000505335.1:p.Asp1759Asn
ENST00000681136.1:n.1514G>A
ENST00000681696.1:c.1213G>A	ENSP00000505871.1:p.Asp405Asn
ENST00000298910.11:c.5530G>A	ENSP00000298910.7:p.Asp1844Asn
ENST00000430804.5:c.2826G>A
ENST00000479187.5:n.2211G>A
NM_198578.3:c.5530G>A	NP_940980.3:p.Asp1844Asn
XM_005268629.2:c.5530G>A	XP_005268686.1:p.Asp1844Asn
XM_011537877.1:c.5530G>A	XP_011536179.1:p.Asp1844Asn
XM_011537878.1:c.5530G>A	XP_011536180.1:p.Asp1844Asn
XM_011537879.1:c.4327G>A	XP_011536181.1:p.Asp1443Asn
XM_005268629.4:c.5530G>A	XP_005268686.1:p.Asp1844Asn
XM_011537877.3:c.5530G>A	XP_011536179.1:p.Asp1844Asn
XM_017018787.1:c.2446G>A	XP_016874276.1:p.Asp816Asn
XM_017018788.2:c.1792G>A	XP_016874277.1:p.Asp598Asn
XM_024448833.1:c.4327G>A	XP_024304601.1:p.Asp1443Asn
NM_198578.4:c.5530G>A MANE Select	NP_940980.4:p.Asp1844Asn