Canonical Allele Identifier: CA2575189068

Gene: LRRK2

Linked Data

• gnomAD v4: 12-40309032-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40309032A>G , CM000674.2:g.40309032A>G	GRCh38
NC_000012.11:g.40702834A>G , CM000674.1:g.40702834A>G	GRCh37
NC_000012.10:g.38989101A>G	NCBI36
NG_011709.1:g.89022A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.4190-74A>G MANE Select	ENSP00000298910.7:n.4190-74A>G
ENST00000679360.1:c.*3099-74A>G	ENSP00000505368.1:n.*3099-74A>G
ENST00000680790.1:c.3935-74A>G	ENSP00000505335.1:n.3935-74A>G
ENST00000298910.11:c.4190-74A>G	ENSP00000298910.7:n.4190-74A>G
ENST00000430804.5:c.1486-74A>G
ENST00000479187.5:n.871-74A>G
NM_198578.3:c.4190-74A>G	NP_940980.3:n.4190-74A>G
XM_005268629.2:c.4190-74A>G	XP_005268686.1:n.4190-74A>G
XM_011537877.1:c.4190-74A>G	XP_011536179.1:n.4190-74A>G
XM_011537878.1:c.4190-74A>G	XP_011536180.1:n.4190-74A>G
XM_011537879.1:c.2987-74A>G	XP_011536181.1:n.2987-74A>G
XM_011537880.1:c.4190-74A>G	XP_011536182.1:n.4190-74A>G
XM_011537881.1:c.4190-74A>G	XP_011536183.1:n.4190-74A>G
XM_005268629.4:c.4190-74A>G	XP_005268686.1:n.4190-74A>G
XM_011537877.3:c.4190-74A>G	XP_011536179.1:n.4190-74A>G
XM_011537881.3:c.4190-74A>G	XP_011536183.1:n.4190-74A>G
XM_017018786.2:c.4190-74A>G	XP_016874275.1:n.4190-74A>G
XM_017018787.1:c.1106-74A>G	XP_016874276.1:n.1106-74A>G
XM_017018788.2:c.452-74A>G	XP_016874277.1:n.452-74A>G
XM_024448833.1:c.2987-74A>G	XP_024304601.1:n.2987-74A>G
XR_001748574.2:n.4432-74A>G
NM_198578.4:c.4190-74A>G MANE Select	NP_940980.4:n.4190-74A>G