Canonical Allele Identifier: CA2618284261
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40320260_40320263del , CM000674.2:g.40320260_40320263del GRCh38
NC_000012.11:g.40714062_40714065del , CM000674.1:g.40714062_40714065del GRCh37
NC_000012.10:g.39000329_39000332del NCBI36
NG_011709.1:g.100250_100253del

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.5015+85_5015+88del MANE Select ENSP00000298910.7:n.5015+85_5015+88del
ENST00000679360.1:c.*3924+85_*3924+88del ENSP00000505368.1:n.*3924+85_*3924+88del
ENST00000679532.1:c.789+85_789+88del
ENST00000680018.1:c.460+85_460+88del ENSP00000505347.1:n.460+85_460+88del
ENST00000680422.1:c.660+85_660+88del
ENST00000680425.1:c.183-774_183-771del ENSP00000506459.1:n.183-774_183-771del
ENST00000680453.1:c.473-774_473-771del
ENST00000680790.1:c.4760+85_4760+88del ENSP00000505335.1:n.4760+85_4760+88del
ENST00000681136.1:n.999+85_999+88del
ENST00000681696.1:c.698+85_698+88del ENSP00000505871.1:n.698+85_698+88del
ENST00000298910.11:c.5015+85_5015+88del ENSP00000298910.7:n.5015+85_5015+88del
ENST00000430804.5:c.2311+85_2311+88del
ENST00000479187.5:n.1696+85_1696+88del
NM_198578.3:c.5015+85_5015+88del NP_940980.3:n.5015+85_5015+88del
XM_005268629.2:c.5015+85_5015+88del XP_005268686.1:n.5015+85_5015+88del
XM_011537877.1:c.5015+85_5015+88del XP_011536179.1:n.5015+85_5015+88del
XM_011537878.1:c.5015+85_5015+88del XP_011536180.1:n.5015+85_5015+88del
XM_011537879.1:c.3812+85_3812+88del XP_011536181.1:n.3812+85_3812+88del
XM_011537881.1:c.4828-774_4828-771del XP_011536183.1:n.4828-774_4828-771del
XM_005268629.4:c.5015+85_5015+88del XP_005268686.1:n.5015+85_5015+88del
XM_011537877.3:c.5015+85_5015+88del XP_011536179.1:n.5015+85_5015+88del
XM_011537881.3:c.4828-774_4828-771del XP_011536183.1:n.4828-774_4828-771del
XM_017018787.1:c.1931+85_1931+88del XP_016874276.1:n.1931+85_1931+88del
XM_017018788.2:c.1277+85_1277+88del XP_016874277.1:n.1277+85_1277+88del
XM_024448833.1:c.3812+85_3812+88del XP_024304601.1:n.3812+85_3812+88del
XR_001748574.2:n.5383+85_5383+88del
NM_198578.4:c.5015+85_5015+88del MANE Select NP_940980.4:n.5015+85_5015+88del