Canonical Allele Identifier: CA2031001047
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs1945448076

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40323072_40323073insATTTT , CM000674.2:g.40323072_40323073insATTTT GRCh38
NC_000012.11:g.40716874_40716875insATTTT , CM000674.1:g.40716874_40716875insATTTT GRCh37
NC_000012.10:g.39003141_39003142insATTTT NCBI36
NG_011709.1:g.103062_103063insATTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5510-88_5510-87insATTTT MANE Select ENSP00000298910.7:n.5510-88_5510-87insATTTT
ENST00000679360.1:c.*4419-88_*4419-87insATTTT ENSP00000505368.1:n.*4419-88_*4419-87insATTTT
ENST00000679532.1:c.1284-88_1284-87insATTTT
ENST00000680018.1:c.955-88_955-87insATTTT ENSP00000505347.1:n.955-88_955-87insATTTT
ENST00000680422.1:c.1155-88_1155-87insATTTT
ENST00000680425.1:c.677-88_677-87insATTTT ENSP00000506459.1:n.677-88_677-87insATTTT
ENST00000680453.1:c.967-88_967-87insATTTT
ENST00000680790.1:c.5255-88_5255-87insATTTT ENSP00000505335.1:n.5255-88_5255-87insATTTT
ENST00000681136.1:n.1494-88_1494-87insATTTT
ENST00000681696.1:c.1193-88_1193-87insATTTT ENSP00000505871.1:n.1193-88_1193-87insATTTT
ENST00000298910.11:c.5510-88_5510-87insATTTT ENSP00000298910.7:n.5510-88_5510-87insATTTT
ENST00000430804.5:c.2806-88_2806-87insATTTT
ENST00000479187.5:n.2191-88_2191-87insATTTT
NM_198578.3:c.5510-88_5510-87insATTTT NP_940980.3:n.5510-88_5510-87insATTTT
XM_005268629.2:c.5510-88_5510-87insATTTT XP_005268686.1:n.5510-88_5510-87insATTTT
XM_011537877.1:c.5510-88_5510-87insATTTT XP_011536179.1:n.5510-88_5510-87insATTTT
XM_011537878.1:c.5510-88_5510-87insATTTT XP_011536180.1:n.5510-88_5510-87insATTTT
XM_011537879.1:c.4307-88_4307-87insATTTT XP_011536181.1:n.4307-88_4307-87insATTTT
XM_005268629.4:c.5510-88_5510-87insATTTT XP_005268686.1:n.5510-88_5510-87insATTTT
XM_011537877.3:c.5510-88_5510-87insATTTT XP_011536179.1:n.5510-88_5510-87insATTTT
XM_017018787.1:c.2426-88_2426-87insATTTT XP_016874276.1:n.2426-88_2426-87insATTTT
XM_017018788.2:c.1772-88_1772-87insATTTT XP_016874277.1:n.1772-88_1772-87insATTTT
XM_024448833.1:c.4307-88_4307-87insATTTT XP_024304601.1:n.4307-88_4307-87insATTTT
NM_198578.4:c.5510-88_5510-87insATTTT MANE Select NP_940980.4:n.5510-88_5510-87insATTTT