Canonical Allele Identifier: CA2031005964

Gene: LRRK2

Linked Data

• dbSNP Id: rs1592269954

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40310364T>G , CM000674.2:g.40310364T>G	GRCh38
NC_000012.11:g.40704166T>G , CM000674.1:g.40704166T>G	GRCh37
NC_000012.10:g.38990433T>G	NCBI36
NG_011709.1:g.90354T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.4318-67T>G MANE Select	ENSP00000298910.7:n.4318-67T>G
ENST00000679360.1:c.*3227-67T>G	ENSP00000505368.1:n.*3227-67T>G
ENST00000680790.1:c.4063-67T>G	ENSP00000505335.1:n.4063-67T>G
ENST00000298910.11:c.4318-67T>G	ENSP00000298910.7:n.4318-67T>G
ENST00000430804.5:c.1614-67T>G
ENST00000479187.5:n.999-67T>G
NM_198578.3:c.4318-67T>G	NP_940980.3:n.4318-67T>G
XM_005268629.2:c.4318-67T>G	XP_005268686.1:n.4318-67T>G
XM_011537877.1:c.4318-67T>G	XP_011536179.1:n.4318-67T>G
XM_011537878.1:c.4318-67T>G	XP_011536180.1:n.4318-67T>G
XM_011537879.1:c.3115-67T>G	XP_011536181.1:n.3115-67T>G
XM_011537880.1:c.4318-67T>G	XP_011536182.1:n.4318-67T>G
XM_011537881.1:c.4318-67T>G	XP_011536183.1:n.4318-67T>G
XM_005268629.4:c.4318-67T>G	XP_005268686.1:n.4318-67T>G
XM_011537877.3:c.4318-67T>G	XP_011536179.1:n.4318-67T>G
XM_011537881.3:c.4318-67T>G	XP_011536183.1:n.4318-67T>G
XM_017018786.2:c.4318-67T>G	XP_016874275.1:n.4318-67T>G
XM_017018787.1:c.1234-67T>G	XP_016874276.1:n.1234-67T>G
XM_017018788.2:c.580-67T>G	XP_016874277.1:n.580-67T>G
XM_024448833.1:c.3115-67T>G	XP_024304601.1:n.3115-67T>G
XR_001748574.2:n.4560-67T>G
NM_198578.4:c.4318-67T>G MANE Select	NP_940980.4:n.4318-67T>G