Canonical Allele Identifier: CA235362142

Gene: LRRK2

Linked Data

• dbSNP Id: rs897135882
• MyVariant Identifiers: chr12:g.40713938C>T (hg19) ; chr12:g.40320136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320136C>T , CM000674.2:g.40320136C>T	GRCh38
NC_000012.11:g.40713938C>T , CM000674.1:g.40713938C>T	GRCh37
NC_000012.10:g.39000205C>T	NCBI36
NG_011709.1:g.100126C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4976C>T MANE Select	ENSP00000298910.7:p.Ala1659Val
ENST00000679360.1:c.*3885C>T	ENSP00000505368.1:n.*3885C>T
ENST00000679532.1:c.750C>T
ENST00000680018.1:c.421C>T	ENSP00000505347.1:n.421C>T
ENST00000680422.1:c.621C>T
ENST00000680425.1:c.183-898C>T	ENSP00000506459.1:n.183-898C>T
ENST00000680453.1:c.473-898C>T
ENST00000680790.1:c.4721C>T	ENSP00000505335.1:p.Ala1574Val
ENST00000681136.1:n.960C>T
ENST00000681696.1:c.659C>T	ENSP00000505871.1:p.Ala220Val
ENST00000298910.11:c.4976C>T	ENSP00000298910.7:p.Ala1659Val
ENST00000430804.5:c.2272C>T
ENST00000479187.5:n.1657C>T
NM_198578.3:c.4976C>T	NP_940980.3:p.Ala1659Val
XM_005268629.2:c.4976C>T	XP_005268686.1:p.Ala1659Val
XM_011537877.1:c.4976C>T	XP_011536179.1:p.Ala1659Val
XM_011537878.1:c.4976C>T	XP_011536180.1:p.Ala1659Val
XM_011537879.1:c.3773C>T	XP_011536181.1:p.Ala1258Val
XM_011537881.1:c.4828-898C>T	XP_011536183.1:n.4828-898C>T
XM_005268629.4:c.4976C>T	XP_005268686.1:p.Ala1659Val
XM_011537877.3:c.4976C>T	XP_011536179.1:p.Ala1659Val
XM_011537881.3:c.4828-898C>T	XP_011536183.1:n.4828-898C>T
XM_017018787.1:c.1892C>T	XP_016874276.1:p.Ala631Val
XM_017018788.2:c.1238C>T	XP_016874277.1:p.Ala413Val
XM_024448833.1:c.3773C>T	XP_024304601.1:p.Ala1258Val
XR_001748574.2:n.5344C>T
NM_198578.4:c.4976C>T MANE Select	NP_940980.4:p.Ala1659Val