Canonical Allele Identifier: CA384417998

Gene: LRRK2

Linked Data

• dbSNP Id: rs941218392
• gnomAD v2: 12-40702925-A-G
• gnomAD v4: 12-40309123-A-G
• MyVariant Identifiers: chr12:g.40702925A>G (hg19) ; chr12:g.40309123A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40309123A>G , CM000674.2:g.40309123A>G	GRCh38
NC_000012.11:g.40702925A>G , CM000674.1:g.40702925A>G	GRCh37
NC_000012.10:g.38989192A>G	NCBI36
NG_011709.1:g.89113A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298910.12:c.4207A>G MANE Select	ENSP00000298910.7:p.Ser1403Gly
ENST00000679360.1:c.*3116A>G	ENSP00000505368.1:n.*3116A>G
ENST00000680790.1:c.3952A>G	ENSP00000505335.1:p.Ser1318Gly
ENST00000298910.11:c.4207A>G	ENSP00000298910.7:p.Ser1403Gly
ENST00000430804.5:c.1503A>G
ENST00000479187.5:n.888A>G
NM_198578.3:c.4207A>G	NP_940980.3:p.Ser1403Gly
XM_005268629.2:c.4207A>G	XP_005268686.1:p.Ser1403Gly
XM_011537877.1:c.4207A>G	XP_011536179.1:p.Ser1403Gly
XM_011537878.1:c.4207A>G	XP_011536180.1:p.Ser1403Gly
XM_011537879.1:c.3004A>G	XP_011536181.1:p.Ser1002Gly
XM_011537880.1:c.4207A>G	XP_011536182.1:p.Ser1403Gly
XM_011537881.1:c.4207A>G	XP_011536183.1:p.Ser1403Gly
XM_005268629.4:c.4207A>G	XP_005268686.1:p.Ser1403Gly
XM_011537877.3:c.4207A>G	XP_011536179.1:p.Ser1403Gly
XM_011537881.3:c.4207A>G	XP_011536183.1:p.Ser1403Gly
XM_017018786.2:c.4207A>G	XP_016874275.1:p.Ser1403Gly
XM_017018787.1:c.1123A>G	XP_016874276.1:p.Ser375Gly
XM_017018788.2:c.469A>G	XP_016874277.1:p.Ser157Gly
XM_024448833.1:c.3004A>G	XP_024304601.1:p.Ser1002Gly
XR_001748574.2:n.4449A>G
NM_198578.4:c.4207A>G MANE Select	NP_940980.4:p.Ser1403Gly