Canonical Allele Identifier: CA235359531

Gene: LRRK2

Linked Data

• dbSNP Id: rs188212126
• gnomAD v3: 12-40363403-T-G
• gnomAD v4: 12-40363403-T-G
• MyVariant Identifiers: chr12:g.40757205T>G (hg19) ; chr12:g.40363403T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40363403T>G , CM000674.2:g.40363403T>G	GRCh38
NC_000012.11:g.40757205T>G , CM000674.1:g.40757205T>G	GRCh37
NC_000012.10:g.39043472T>G	NCBI36
NG_011709.1:g.143393T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.7030T>G MANE Select	ENSP00000298910.7:p.Phe2344Val
ENST00000636518.1:c.827T>G
ENST00000679360.1:c.*5939T>G	ENSP00000505368.1:n.*5939T>G
ENST00000679532.1:c.2804T>G
ENST00000679683.1:c.820T>G
ENST00000680018.1:c.2475T>G	ENSP00000505347.1:n.2475T>G
ENST00000680422.1:c.4117T>G
ENST00000680425.1:c.2197T>G	ENSP00000506459.1:n.2197T>G
ENST00000680453.1:c.2487T>G
ENST00000680790.1:c.6775T>G	ENSP00000505335.1:p.Phe2259Val
ENST00000681136.1:n.3014T>G
ENST00000681696.1:c.2713T>G	ENSP00000505871.1:p.Phe905Val
ENST00000681773.1:n.237T>G
ENST00000298910.11:c.7030T>G	ENSP00000298910.7:p.Phe2344Val
ENST00000430804.5:c.4326T>G
ENST00000479187.5:n.3711T>G
NM_198578.3:c.7030T>G	NP_940980.3:p.Phe2344Val
XM_005268629.2:c.7030T>G	XP_005268686.1:p.Phe2344Val
XM_011537877.1:c.7030T>G	XP_011536179.1:p.Phe2344Val
XM_011537879.1:c.5827T>G	XP_011536181.1:p.Phe1943Val
XR_944868.1:n.485-8576A>C
XM_005268629.4:c.7030T>G	XP_005268686.1:p.Phe2344Val
XM_011537877.3:c.7030T>G	XP_011536179.1:p.Phe2344Val
XM_017018787.1:c.3946T>G	XP_016874276.1:p.Phe1316Val
XM_017018788.2:c.3292T>G	XP_016874277.1:p.Phe1098Val
XM_024448833.1:c.5827T>G	XP_024304601.1:p.Phe1943Val
XR_944868.2:n.485-8576A>C
NM_198578.4:c.7030T>G MANE Select	NP_940980.4:p.Phe2344Val