Canonical Allele Identifier: CA384419696

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40713931C>G (hg19) ; chr12:g.40320129C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40320129C>G , CM000674.2:g.40320129C>G	GRCh38
NC_000012.11:g.40713931C>G , CM000674.1:g.40713931C>G	GRCh37
NC_000012.10:g.39000198C>G	NCBI36
NG_011709.1:g.100119C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4969C>G MANE Select	ENSP00000298910.7:p.Gln1657Glu
ENST00000679360.1:c.*3878C>G	ENSP00000505368.1:n.*3878C>G
ENST00000679532.1:c.743C>G
ENST00000680018.1:c.414C>G	ENSP00000505347.1:n.414C>G
ENST00000680422.1:c.614C>G
ENST00000680425.1:c.183-905C>G	ENSP00000506459.1:n.183-905C>G
ENST00000680453.1:c.473-905C>G
ENST00000680790.1:c.4714C>G	ENSP00000505335.1:p.Gln1572Glu
ENST00000681136.1:n.953C>G
ENST00000681696.1:c.652C>G	ENSP00000505871.1:p.Gln218Glu
ENST00000298910.11:c.4969C>G	ENSP00000298910.7:p.Gln1657Glu
ENST00000430804.5:c.2265C>G
ENST00000479187.5:n.1650C>G
NM_198578.3:c.4969C>G	NP_940980.3:p.Gln1657Glu
XM_005268629.2:c.4969C>G	XP_005268686.1:p.Gln1657Glu
XM_011537877.1:c.4969C>G	XP_011536179.1:p.Gln1657Glu
XM_011537878.1:c.4969C>G	XP_011536180.1:p.Gln1657Glu
XM_011537879.1:c.3766C>G	XP_011536181.1:p.Gln1256Glu
XM_011537881.1:c.4828-905C>G	XP_011536183.1:n.4828-905C>G
XM_005268629.4:c.4969C>G	XP_005268686.1:p.Gln1657Glu
XM_011537877.3:c.4969C>G	XP_011536179.1:p.Gln1657Glu
XM_011537881.3:c.4828-905C>G	XP_011536183.1:n.4828-905C>G
XM_017018787.1:c.1885C>G	XP_016874276.1:p.Gln629Glu
XM_017018788.2:c.1231C>G	XP_016874277.1:p.Gln411Glu
XM_024448833.1:c.3766C>G	XP_024304601.1:p.Gln1256Glu
XR_001748574.2:n.5337C>G
NM_198578.4:c.4969C>G MANE Select	NP_940980.4:p.Gln1657Glu