Canonical Allele Identifier: CA384413579

Gene: LRRK2

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.7163A>C MANE Select	ENSP00000298910.7:p.Asp2388Ala
ENST00000636518.1:c.960A>C
ENST00000679360.1:c.*6072A>C	ENSP00000505368.1:n.*6072A>C
ENST00000679532.1:c.2937A>C
ENST00000679683.1:c.953A>C
ENST00000680018.1:c.2608A>C	ENSP00000505347.1:n.2608A>C
ENST00000680422.1:c.4250A>C
ENST00000680425.1:c.2330A>C	ENSP00000506459.1:n.2330A>C
ENST00000680453.1:c.2620A>C
ENST00000680790.1:c.6908A>C	ENSP00000505335.1:p.Asp2303Ala
ENST00000681136.1:n.3147A>C
ENST00000681696.1:c.2846A>C	ENSP00000505871.1:p.Asp949Ala
ENST00000681773.1:n.370A>C
ENST00000298910.11:c.7163A>C	ENSP00000298910.7:p.Asp2388Ala
ENST00000430804.5:c.4459A>C
ENST00000479187.5:n.3844A>C
NM_198578.3:c.7163A>C	NP_940980.3:p.Asp2388Ala
XM_005268629.2:c.7163A>C	XP_005268686.1:p.Asp2388Ala
XM_011537877.1:c.7163A>C	XP_011536179.1:p.Asp2388Ala
XM_011537879.1:c.5960A>C	XP_011536181.1:p.Asp1987Ala
XR_944868.1:n.485-8709T>G
XM_005268629.4:c.7163A>C	XP_005268686.1:p.Asp2388Ala
XM_011537877.3:c.7163A>C	XP_011536179.1:p.Asp2388Ala
XM_017018787.1:c.4079A>C	XP_016874276.1:p.Asp1360Ala
XM_017018788.2:c.3425A>C	XP_016874277.1:p.Asp1142Ala
XM_024448833.1:c.5960A>C	XP_024304601.1:p.Asp1987Ala
XR_944868.2:n.485-8709T>G
NM_198578.4:c.7163A>C MANE Select	NP_940980.4:p.Asp2388Ala