Canonical Allele Identifier: CA384413580

Gene: LRRK2

Linked Data

• MyVariant Identifiers: chr12:g.40757338A>T (hg19) ; chr12:g.40363536A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363536A>T , CM000674.2:g.40363536A>T	GRCh38
NC_000012.11:g.40757338A>T , CM000674.1:g.40757338A>T	GRCh37
NC_000012.10:g.39043605A>T	NCBI36
NG_011709.1:g.143526A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7163A>T MANE Select	ENSP00000298910.7:p.Asp2388Val
ENST00000636518.1:c.960A>T
ENST00000679360.1:c.*6072A>T	ENSP00000505368.1:n.*6072A>T
ENST00000679532.1:c.2937A>T
ENST00000679683.1:c.953A>T
ENST00000680018.1:c.2608A>T	ENSP00000505347.1:n.2608A>T
ENST00000680422.1:c.4250A>T
ENST00000680425.1:c.2330A>T	ENSP00000506459.1:n.2330A>T
ENST00000680453.1:c.2620A>T
ENST00000680790.1:c.6908A>T	ENSP00000505335.1:p.Asp2303Val
ENST00000681136.1:n.3147A>T
ENST00000681696.1:c.2846A>T	ENSP00000505871.1:p.Asp949Val
ENST00000681773.1:n.370A>T
ENST00000298910.11:c.7163A>T	ENSP00000298910.7:p.Asp2388Val
ENST00000430804.5:c.4459A>T
ENST00000479187.5:n.3844A>T
NM_198578.3:c.7163A>T	NP_940980.3:p.Asp2388Val
XM_005268629.2:c.7163A>T	XP_005268686.1:p.Asp2388Val
XM_011537877.1:c.7163A>T	XP_011536179.1:p.Asp2388Val
XM_011537879.1:c.5960A>T	XP_011536181.1:p.Asp1987Val
XR_944868.1:n.485-8709T>A
XM_005268629.4:c.7163A>T	XP_005268686.1:p.Asp2388Val
XM_011537877.3:c.7163A>T	XP_011536179.1:p.Asp2388Val
XM_017018787.1:c.4079A>T	XP_016874276.1:p.Asp1360Val
XM_017018788.2:c.3425A>T	XP_016874277.1:p.Asp1142Val
XM_024448833.1:c.5960A>T	XP_024304601.1:p.Asp1987Val
XR_944868.2:n.485-8709T>A
NM_198578.4:c.7163A>T MANE Select	NP_940980.4:p.Asp2388Val