Canonical Allele Identifier: CA2575189067

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40309022T>A , CM000674.2:g.40309022T>A	GRCh38
NC_000012.11:g.40702824T>A , CM000674.1:g.40702824T>A	GRCh37
NC_000012.10:g.38989091T>A	NCBI36
NG_011709.1:g.89012T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.4190-84T>A MANE Select	ENSP00000298910.7:n.4190-84T>A
ENST00000679360.1:c.*3099-84T>A	ENSP00000505368.1:n.*3099-84T>A
ENST00000680790.1:c.3935-84T>A	ENSP00000505335.1:n.3935-84T>A
ENST00000298910.11:c.4190-84T>A	ENSP00000298910.7:n.4190-84T>A
ENST00000430804.5:c.1486-84T>A
ENST00000479187.5:n.871-84T>A
NM_198578.3:c.4190-84T>A	NP_940980.3:n.4190-84T>A
XM_005268629.2:c.4190-84T>A	XP_005268686.1:n.4190-84T>A
XM_011537877.1:c.4190-84T>A	XP_011536179.1:n.4190-84T>A
XM_011537878.1:c.4190-84T>A	XP_011536180.1:n.4190-84T>A
XM_011537879.1:c.2987-84T>A	XP_011536181.1:n.2987-84T>A
XM_011537880.1:c.4190-84T>A	XP_011536182.1:n.4190-84T>A
XM_011537881.1:c.4190-84T>A	XP_011536183.1:n.4190-84T>A
XM_005268629.4:c.4190-84T>A	XP_005268686.1:n.4190-84T>A
XM_011537877.3:c.4190-84T>A	XP_011536179.1:n.4190-84T>A
XM_011537881.3:c.4190-84T>A	XP_011536183.1:n.4190-84T>A
XM_017018786.2:c.4190-84T>A	XP_016874275.1:n.4190-84T>A
XM_017018787.1:c.1106-84T>A	XP_016874276.1:n.1106-84T>A
XM_017018788.2:c.452-84T>A	XP_016874277.1:n.452-84T>A
XM_024448833.1:c.2987-84T>A	XP_024304601.1:n.2987-84T>A
XR_001748574.2:n.4432-84T>A
NM_198578.4:c.4190-84T>A MANE Select	NP_940980.4:n.4190-84T>A