Canonical Allele Identifier: CA6513865
Gene: LRRK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1729983
ClinVar RCV Id: RCV002326224
dbSNP Id: rs766332077

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40298447A>G , CM000674.2:g.40298447A>G GRCh38
NC_000012.11:g.40692249A>G , CM000674.1:g.40692249A>G GRCh37
NC_000012.10:g.38978516A>G NCBI36
NG_011709.1:g.78437A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.3301A>G MANE Select ENSP00000298910.7:p.Asn1101Asp
ENST00000679360.1:c.*2210A>G ENSP00000505368.1:n.*2210A>G
ENST00000680790.1:c.3046A>G ENSP00000505335.1:p.Asn1016Asp
ENST00000298910.11:c.3301A>G ENSP00000298910.7:p.Asn1101Asp
ENST00000343742.6:c.3301A>G ENSP00000341930.2:p.Asn1101Asp
ENST00000430804.5:c.345A>G
NM_198578.3:c.3301A>G NP_940980.3:p.Asn1101Asp
XM_005268629.2:c.3301A>G XP_005268686.1:p.Asn1101Asp
XM_011537877.1:c.3301A>G XP_011536179.1:p.Asn1101Asp
XM_011537878.1:c.3301A>G XP_011536180.1:p.Asn1101Asp
XM_011537879.1:c.2098A>G XP_011536181.1:p.Asn700Asp
XM_011537880.1:c.3301A>G XP_011536182.1:p.Asn1101Asp
XM_011537881.1:c.3301A>G XP_011536183.1:p.Asn1101Asp
XM_011537882.1:c.3301A>G XP_011536184.1:p.Asn1101Asp
XM_005268629.4:c.3301A>G XP_005268686.1:p.Asn1101Asp
XM_011537877.3:c.3301A>G XP_011536179.1:p.Asn1101Asp
XM_011537881.3:c.3301A>G XP_011536183.1:p.Asn1101Asp
XM_011537882.3:c.3301A>G XP_011536184.1:p.Asn1101Asp
XM_017018786.2:c.3301A>G XP_016874275.1:p.Asn1101Asp
XM_017018787.1:c.217A>G XP_016874276.1:p.Asn73Asp
XM_017018789.2:c.3301A>G XP_016874278.1:p.Asn1101Asp
XM_024448833.1:c.2098A>G XP_024304601.1:p.Asn700Asp
XR_001748574.2:n.3543A>G
NM_198578.4:c.3301A>G MANE Select NP_940980.4:p.Asn1101Asp