Canonical Allele Identifier: CA384419817

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40321039-C-G
• MyVariant Identifiers: chr12:g.40714841C>G (hg19) ; chr12:g.40321039C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40321039C>G , CM000674.2:g.40321039C>G	GRCh38
NC_000012.11:g.40714841C>G , CM000674.1:g.40714841C>G	GRCh37
NC_000012.10:g.39001108C>G	NCBI36
NG_011709.1:g.101029C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.5021C>G MANE Select	ENSP00000298910.7:p.Ser1674Cys
ENST00000679360.1:c.*3930C>G	ENSP00000505368.1:n.*3930C>G
ENST00000679532.1:c.795C>G
ENST00000680018.1:c.466C>G	ENSP00000505347.1:n.466C>G
ENST00000680422.1:c.666C>G
ENST00000680425.1:c.188C>G	ENSP00000506459.1:n.188C>G
ENST00000680453.1:c.478C>G
ENST00000680790.1:c.4766C>G	ENSP00000505335.1:p.Ser1589Cys
ENST00000681136.1:n.1005C>G
ENST00000681696.1:c.704C>G	ENSP00000505871.1:p.Ser235Cys
ENST00000298910.11:c.5021C>G	ENSP00000298910.7:p.Ser1674Cys
ENST00000430804.5:c.2317C>G
ENST00000479187.5:n.1702C>G
NM_198578.3:c.5021C>G	NP_940980.3:p.Ser1674Cys
XM_005268629.2:c.5021C>G	XP_005268686.1:p.Ser1674Cys
XM_011537877.1:c.5021C>G	XP_011536179.1:p.Ser1674Cys
XM_011537878.1:c.5021C>G	XP_011536180.1:p.Ser1674Cys
XM_011537879.1:c.3818C>G	XP_011536181.1:p.Ser1273Cys
XM_011537881.1:c.4833C>G	XP_011536183.1:p.Val1611=
XM_005268629.4:c.5021C>G	XP_005268686.1:p.Ser1674Cys
XM_011537877.3:c.5021C>G	XP_011536179.1:p.Ser1674Cys
XM_011537881.3:c.4833C>G	XP_011536183.1:p.Val1611=
XM_017018787.1:c.1937C>G	XP_016874276.1:p.Ser646Cys
XM_017018788.2:c.1283C>G	XP_016874277.1:p.Ser428Cys
XM_024448833.1:c.3818C>G	XP_024304601.1:p.Ser1273Cys
XR_001748574.2:n.5389C>G
NM_198578.4:c.5021C>G MANE Select	NP_940980.4:p.Ser1674Cys