Canonical Allele Identifier: CA384404109

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40734230G>T (hg19) ; chr12:g.40340428G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40340428G>T , CM000674.2:g.40340428G>T	GRCh38
NC_000012.11:g.40734230G>T , CM000674.1:g.40734230G>T	GRCh37
NC_000012.10:g.39020497G>T	NCBI36
NG_011709.1:g.120418G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.6083G>T MANE Select	ENSP00000298910.7:p.Gly2028Val
ENST00000679360.1:c.*4992G>T	ENSP00000505368.1:n.*4992G>T
ENST00000679532.1:c.1857G>T
ENST00000680018.1:c.1528G>T	ENSP00000505347.1:n.1528G>T
ENST00000680422.1:c.1728G>T
ENST00000680425.1:c.1250G>T	ENSP00000506459.1:n.1250G>T
ENST00000680453.1:c.1540G>T
ENST00000680790.1:c.5828G>T	ENSP00000505335.1:p.Gly1943Val
ENST00000681136.1:n.2067G>T
ENST00000681696.1:c.1766G>T	ENSP00000505871.1:p.Gly589Val
ENST00000298910.11:c.6083G>T	ENSP00000298910.7:p.Gly2028Val
ENST00000430804.5:c.3379G>T
ENST00000479187.5:n.2764G>T
NM_198578.3:c.6083G>T	NP_940980.3:p.Gly2028Val
XM_005268629.2:c.6083G>T	XP_005268686.1:p.Gly2028Val
XM_011537877.1:c.6083G>T	XP_011536179.1:p.Gly2028Val
XM_011537878.1:c.6083G>T	XP_011536180.1:p.Gly2028Val
XM_011537879.1:c.4880G>T	XP_011536181.1:p.Gly1627Val
XM_005268629.4:c.6083G>T	XP_005268686.1:p.Gly2028Val
XM_011537877.3:c.6083G>T	XP_011536179.1:p.Gly2028Val
XM_017018787.1:c.2999G>T	XP_016874276.1:p.Gly1000Val
XM_017018788.2:c.2345G>T	XP_016874277.1:p.Gly782Val
XM_024448833.1:c.4880G>T	XP_024304601.1:p.Gly1627Val
NM_198578.4:c.6083G>T MANE Select	NP_940980.4:p.Gly2028Val