Canonical Allele Identifier: CA6513286

Gene: LRRK2

Linked Data

• ClinVar Variation Id: 308613
• ClinVar RCV Id: RCV000281737 ; RCV001594942 ; RCV001580119
• dbSNP Id: rs7955902
• ExAC: 12:40645257 C / A
• gnomAD v2: 12-40645257-C-A
• gnomAD v3: 12-40251455-C-A
• gnomAD v4: 12-40251455-C-A
• MyVariant Identifiers: chr12:g.40645257C>A (hg19) ; chr12:g.40251455C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40251455C>A , CM000674.2:g.40251455C>A	GRCh38
NC_000012.11:g.40645257C>A , CM000674.1:g.40645257C>A	GRCh37
NC_000012.10:g.38931524C>A	NCBI36
NG_011709.1:g.31445C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.1102-10C>A MANE Select	ENSP00000298910.7:n.1102-10C>A
ENST00000644108.1:c.1072-10C>A
ENST00000679360.1:c.1102-10C>A	ENSP00000505368.1:n.1102-10C>A
ENST00000680790.1:c.1102-10C>A	ENSP00000505335.1:n.1102-10C>A
ENST00000298910.11:c.1102-10C>A	ENSP00000298910.7:n.1102-10C>A
ENST00000343742.6:c.1102-10C>A	ENSP00000341930.2:n.1102-10C>A
ENST00000416796.5:c.611-1510C>A	ENSP00000398726.1:n.611-1510C>A
NM_198578.3:c.1102-10C>A	NP_940980.3:n.1102-10C>A
XM_005268629.2:c.1102-10C>A	XP_005268686.1:n.1102-10C>A
XM_011537877.1:c.1102-10C>A	XP_011536179.1:n.1102-10C>A
XM_011537878.1:c.1102-10C>A	XP_011536180.1:n.1102-10C>A
XM_011537880.1:c.1102-10C>A	XP_011536182.1:n.1102-10C>A
XM_011537881.1:c.1102-10C>A	XP_011536183.1:n.1102-10C>A
XM_011537882.1:c.1102-10C>A	XP_011536184.1:n.1102-10C>A
XM_005268629.4:c.1102-10C>A	XP_005268686.1:n.1102-10C>A
XM_011537877.3:c.1102-10C>A	XP_011536179.1:n.1102-10C>A
XM_011537881.3:c.1102-10C>A	XP_011536183.1:n.1102-10C>A
XM_011537882.3:c.1102-10C>A	XP_011536184.1:n.1102-10C>A
XM_017018786.2:c.1102-10C>A	XP_016874275.1:n.1102-10C>A
XM_017018789.2:c.1102-10C>A	XP_016874278.1:n.1102-10C>A
XR_001748574.2:n.1344-10C>A
NM_198578.4:c.1102-10C>A MANE Select	NP_940980.4:n.1102-10C>A