Canonical Allele Identifier: CA384419633

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713905A>T (hg19) ; chr12:g.40320103A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320103A>T , CM000674.2:g.40320103A>T	GRCh38
NC_000012.11:g.40713905A>T , CM000674.1:g.40713905A>T	GRCh37
NC_000012.10:g.39000172A>T	NCBI36
NG_011709.1:g.100093A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4943A>T MANE Select	ENSP00000298910.7:p.Gln1648Leu
ENST00000679360.1:c.*3852A>T	ENSP00000505368.1:n.*3852A>T
ENST00000679532.1:c.717A>T
ENST00000680018.1:c.388A>T	ENSP00000505347.1:n.388A>T
ENST00000680422.1:c.588A>T
ENST00000680425.1:c.183-931A>T	ENSP00000506459.1:n.183-931A>T
ENST00000680453.1:c.473-931A>T
ENST00000680790.1:c.4688A>T	ENSP00000505335.1:p.Gln1563Leu
ENST00000681136.1:n.927A>T
ENST00000681696.1:c.626A>T	ENSP00000505871.1:p.Gln209Leu
ENST00000298910.11:c.4943A>T	ENSP00000298910.7:p.Gln1648Leu
ENST00000430804.5:c.2239A>T
ENST00000479187.5:n.1624A>T
NM_198578.3:c.4943A>T	NP_940980.3:p.Gln1648Leu
XM_005268629.2:c.4943A>T	XP_005268686.1:p.Gln1648Leu
XM_011537877.1:c.4943A>T	XP_011536179.1:p.Gln1648Leu
XM_011537878.1:c.4943A>T	XP_011536180.1:p.Gln1648Leu
XM_011537879.1:c.3740A>T	XP_011536181.1:p.Gln1247Leu
XM_011537881.1:c.4828-931A>T	XP_011536183.1:n.4828-931A>T
XM_005268629.4:c.4943A>T	XP_005268686.1:p.Gln1648Leu
XM_011537877.3:c.4943A>T	XP_011536179.1:p.Gln1648Leu
XM_011537881.3:c.4828-931A>T	XP_011536183.1:n.4828-931A>T
XM_017018787.1:c.1859A>T	XP_016874276.1:p.Gln620Leu
XM_017018788.2:c.1205A>T	XP_016874277.1:p.Gln402Leu
XM_024448833.1:c.3740A>T	XP_024304601.1:p.Gln1247Leu
XR_001748574.2:n.5311A>T
NM_198578.4:c.4943A>T MANE Select	NP_940980.4:p.Gln1648Leu