Canonical Allele Identifier: CA604503112

Gene: LRRK2

Linked Data

• dbSNP Id: rs1455759000
• gnomAD v2: 12-40693100-A-G
• gnomAD v4: 12-40299298-A-G
• MyVariant Identifiers: chr12:g.40693100A>G (hg19) ; chr12:g.40299298A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40299298A>G , CM000674.2:g.40299298A>G	GRCh38
NC_000012.11:g.40693100A>G , CM000674.1:g.40693100A>G	GRCh37
NC_000012.10:g.38979367A>G	NCBI36
NG_011709.1:g.79288A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3496+41A>G MANE Select	ENSP00000298910.7:n.3496+41A>G
ENST00000679360.1:c.*2405+41A>G	ENSP00000505368.1:n.*2405+41A>G
ENST00000680790.1:c.3241+41A>G	ENSP00000505335.1:n.3241+41A>G
ENST00000298910.11:c.3496+41A>G	ENSP00000298910.7:n.3496+41A>G
ENST00000343742.6:c.3496+41A>G	ENSP00000341930.2:n.3496+41A>G
ENST00000430804.5:c.540+41A>G
ENST00000479187.5:n.177+41A>G
NM_198578.3:c.3496+41A>G	NP_940980.3:n.3496+41A>G
XM_005268629.2:c.3496+41A>G	XP_005268686.1:n.3496+41A>G
XM_011537877.1:c.3496+41A>G	XP_011536179.1:n.3496+41A>G
XM_011537878.1:c.3496+41A>G	XP_011536180.1:n.3496+41A>G
XM_011537879.1:c.2293+41A>G	XP_011536181.1:n.2293+41A>G
XM_011537880.1:c.3496+41A>G	XP_011536182.1:n.3496+41A>G
XM_011537881.1:c.3496+41A>G	XP_011536183.1:n.3496+41A>G
XM_011537882.1:c.3496+41A>G	XP_011536184.1:n.3496+41A>G
XM_005268629.4:c.3496+41A>G	XP_005268686.1:n.3496+41A>G
XM_011537877.3:c.3496+41A>G	XP_011536179.1:n.3496+41A>G
XM_011537881.3:c.3496+41A>G	XP_011536183.1:n.3496+41A>G
XM_011537882.3:c.3496+41A>G	XP_011536184.1:n.3496+41A>G
XM_017018786.2:c.3496+41A>G	XP_016874275.1:n.3496+41A>G
XM_017018787.1:c.412+41A>G	XP_016874276.1:n.412+41A>G
XM_017018789.2:c.3496+41A>G	XP_016874278.1:n.3496+41A>G
XM_024448833.1:c.2293+41A>G	XP_024304601.1:n.2293+41A>G
XR_001748574.2:n.3738+41A>G
NM_198578.4:c.3496+41A>G MANE Select	NP_940980.4:n.3496+41A>G