Canonical Allele Identifier: CA384418015

Gene: LRRK2

Linked Data

• dbSNP Id: rs1414844149
• gnomAD v2: 12-40702934-C-A
• gnomAD v4: 12-40309132-C-A
• MyVariant Identifiers: chr12:g.40702934C>A (hg19) ; chr12:g.40309132C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40309132C>A , CM000674.2:g.40309132C>A	GRCh38
NC_000012.11:g.40702934C>A , CM000674.1:g.40702934C>A	GRCh37
NC_000012.10:g.38989201C>A	NCBI36
NG_011709.1:g.89122C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.4216C>A MANE Select	ENSP00000298910.7:p.Pro1406Thr
ENST00000679360.1:c.*3125C>A	ENSP00000505368.1:n.*3125C>A
ENST00000680790.1:c.3961C>A	ENSP00000505335.1:p.Pro1321Thr
ENST00000298910.11:c.4216C>A	ENSP00000298910.7:p.Pro1406Thr
ENST00000430804.5:c.1512C>A
ENST00000479187.5:n.897C>A
NM_198578.3:c.4216C>A	NP_940980.3:p.Pro1406Thr
XM_005268629.2:c.4216C>A	XP_005268686.1:p.Pro1406Thr
XM_011537877.1:c.4216C>A	XP_011536179.1:p.Pro1406Thr
XM_011537878.1:c.4216C>A	XP_011536180.1:p.Pro1406Thr
XM_011537879.1:c.3013C>A	XP_011536181.1:p.Pro1005Thr
XM_011537880.1:c.4216C>A	XP_011536182.1:p.Pro1406Thr
XM_011537881.1:c.4216C>A	XP_011536183.1:p.Pro1406Thr
XM_005268629.4:c.4216C>A	XP_005268686.1:p.Pro1406Thr
XM_011537877.3:c.4216C>A	XP_011536179.1:p.Pro1406Thr
XM_011537881.3:c.4216C>A	XP_011536183.1:p.Pro1406Thr
XM_017018786.2:c.4216C>A	XP_016874275.1:p.Pro1406Thr
XM_017018787.1:c.1132C>A	XP_016874276.1:p.Pro378Thr
XM_017018788.2:c.478C>A	XP_016874277.1:p.Pro160Thr
XM_024448833.1:c.3013C>A	XP_024304601.1:p.Pro1005Thr
XR_001748574.2:n.4458C>A
NM_198578.4:c.4216C>A MANE Select	NP_940980.4:p.Pro1406Thr