Canonical Allele Identifier: CA384416002

Gene: LRRK2

Linked Data

• ClinVar Variation Id: 3229615
• ClinVar RCV Id: RCV004525191
• dbSNP Id: rs1226030072
• gnomAD v2: 12-40693050-A-T
• gnomAD v4: 12-40299248-A-T
• MyVariant Identifiers: chr12:g.40693050A>T (hg19) ; chr12:g.40299248A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40299248A>T , CM000674.2:g.40299248A>T	GRCh38
NC_000012.11:g.40693050A>T , CM000674.1:g.40693050A>T	GRCh37
NC_000012.10:g.38979317A>T	NCBI36
NG_011709.1:g.79238A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3487A>T MANE Select	ENSP00000298910.7:p.Asn1163Tyr
ENST00000679360.1:c.*2396A>T	ENSP00000505368.1:n.*2396A>T
ENST00000680790.1:c.3232A>T	ENSP00000505335.1:p.Asn1078Tyr
ENST00000298910.11:c.3487A>T	ENSP00000298910.7:p.Asn1163Tyr
ENST00000343742.6:c.3487A>T	ENSP00000341930.2:p.Asn1163Tyr
ENST00000430804.5:c.531A>T
ENST00000479187.5:n.168A>T
NM_198578.3:c.3487A>T	NP_940980.3:p.Asn1163Tyr
XM_005268629.2:c.3487A>T	XP_005268686.1:p.Asn1163Tyr
XM_011537877.1:c.3487A>T	XP_011536179.1:p.Asn1163Tyr
XM_011537878.1:c.3487A>T	XP_011536180.1:p.Asn1163Tyr
XM_011537879.1:c.2284A>T	XP_011536181.1:p.Asn762Tyr
XM_011537880.1:c.3487A>T	XP_011536182.1:p.Asn1163Tyr
XM_011537881.1:c.3487A>T	XP_011536183.1:p.Asn1163Tyr
XM_011537882.1:c.3487A>T	XP_011536184.1:p.Asn1163Tyr
XM_005268629.4:c.3487A>T	XP_005268686.1:p.Asn1163Tyr
XM_011537877.3:c.3487A>T	XP_011536179.1:p.Asn1163Tyr
XM_011537881.3:c.3487A>T	XP_011536183.1:p.Asn1163Tyr
XM_011537882.3:c.3487A>T	XP_011536184.1:p.Asn1163Tyr
XM_017018786.2:c.3487A>T	XP_016874275.1:p.Asn1163Tyr
XM_017018787.1:c.403A>T	XP_016874276.1:p.Asn135Tyr
XM_017018789.2:c.3487A>T	XP_016874278.1:p.Asn1163Tyr
XM_024448833.1:c.2284A>T	XP_024304601.1:p.Asn762Tyr
XR_001748574.2:n.3729A>T
NM_198578.4:c.3487A>T MANE Select	NP_940980.4:p.Asn1163Tyr