Canonical Allele Identifier: CA688733991

Gene: LRRK2

Linked Data

• dbSNP Id: rs1183933005
• gnomAD v3: 12-40363204-A-G
• gnomAD v4: 12-40363204-A-G
• MyVariant Identifiers: chr12:g.40757006A>G (hg19) ; chr12:g.40363204A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363204A>G , CM000674.2:g.40363204A>G	GRCh38
NC_000012.11:g.40757006A>G , CM000674.1:g.40757006A>G	GRCh37
NC_000012.10:g.39043273A>G	NCBI36
NG_011709.1:g.143194A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7029-198A>G MANE Select	ENSP00000298910.7:n.7029-198A>G
ENST00000636518.1:c.826-198A>G
ENST00000679360.1:c.*5938-198A>G	ENSP00000505368.1:n.*5938-198A>G
ENST00000679532.1:c.2803-198A>G
ENST00000679683.1:c.819-198A>G
ENST00000680018.1:c.2474-198A>G	ENSP00000505347.1:n.2474-198A>G
ENST00000680422.1:c.4116-198A>G
ENST00000680425.1:c.2196-198A>G	ENSP00000506459.1:n.2196-198A>G
ENST00000680453.1:c.2486-198A>G
ENST00000680790.1:c.6774-198A>G	ENSP00000505335.1:n.6774-198A>G
ENST00000681136.1:n.3013-198A>G
ENST00000681696.1:c.2712-198A>G	ENSP00000505871.1:n.2712-198A>G
ENST00000681773.1:n.236-198A>G
ENST00000298910.11:c.7029-198A>G	ENSP00000298910.7:n.7029-198A>G
ENST00000430804.5:c.4325-198A>G
ENST00000479187.5:n.3710-198A>G
NM_198578.3:c.7029-198A>G	NP_940980.3:n.7029-198A>G
XM_005268629.2:c.7029-198A>G	XP_005268686.1:n.7029-198A>G
XM_011537877.1:c.7029-198A>G	XP_011536179.1:n.7029-198A>G
XM_011537878.1:c.*679A>G	XP_011536180.1:n.*679A>G
XM_011537879.1:c.5826-198A>G	XP_011536181.1:n.5826-198A>G
XR_944868.1:n.485-8377T>C
XM_005268629.4:c.7029-198A>G	XP_005268686.1:n.7029-198A>G
XM_011537877.3:c.7029-198A>G	XP_011536179.1:n.7029-198A>G
XM_017018787.1:c.3945-198A>G	XP_016874276.1:n.3945-198A>G
XM_017018788.2:c.3291-198A>G	XP_016874277.1:n.3291-198A>G
XM_024448833.1:c.5826-198A>G	XP_024304601.1:n.5826-198A>G
XR_944868.2:n.485-8377T>C
NM_198578.4:c.7029-198A>G MANE Select	NP_940980.4:n.7029-198A>G