Canonical Allele Identifier: CA384413509

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757317A>T (hg19) ; chr12:g.40363515A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363515A>T , CM000674.2:g.40363515A>T	GRCh38
NC_000012.11:g.40757317A>T , CM000674.1:g.40757317A>T	GRCh37
NC_000012.10:g.39043584A>T	NCBI36
NG_011709.1:g.143505A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7142A>T MANE Select	ENSP00000298910.7:p.Glu2381Val
ENST00000636518.1:c.939A>T
ENST00000679360.1:c.*6051A>T	ENSP00000505368.1:n.*6051A>T
ENST00000679532.1:c.2916A>T
ENST00000679683.1:c.932A>T
ENST00000680018.1:c.2587A>T	ENSP00000505347.1:n.2587A>T
ENST00000680422.1:c.4229A>T
ENST00000680425.1:c.2309A>T	ENSP00000506459.1:n.2309A>T
ENST00000680453.1:c.2599A>T
ENST00000680790.1:c.6887A>T	ENSP00000505335.1:p.Glu2296Val
ENST00000681136.1:n.3126A>T
ENST00000681696.1:c.2825A>T	ENSP00000505871.1:p.Glu942Val
ENST00000681773.1:n.349A>T
ENST00000298910.11:c.7142A>T	ENSP00000298910.7:p.Glu2381Val
ENST00000430804.5:c.4438A>T
ENST00000479187.5:n.3823A>T
NM_198578.3:c.7142A>T	NP_940980.3:p.Glu2381Val
XM_005268629.2:c.7142A>T	XP_005268686.1:p.Glu2381Val
XM_011537877.1:c.7142A>T	XP_011536179.1:p.Glu2381Val
XM_011537879.1:c.5939A>T	XP_011536181.1:p.Glu1980Val
XR_944868.1:n.485-8688T>A
XM_005268629.4:c.7142A>T	XP_005268686.1:p.Glu2381Val
XM_011537877.3:c.7142A>T	XP_011536179.1:p.Glu2381Val
XM_017018787.1:c.4058A>T	XP_016874276.1:p.Glu1353Val
XM_017018788.2:c.3404A>T	XP_016874277.1:p.Glu1135Val
XM_024448833.1:c.5939A>T	XP_024304601.1:p.Glu1980Val
XR_944868.2:n.485-8688T>A
NM_198578.4:c.7142A>T MANE Select	NP_940980.4:p.Glu2381Val