Canonical Allele Identifier: CA2031025614
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363381_40363382delinsTC , CM000674.2:g.40363381_40363382delinsTC GRCh38
NC_000012.11:g.40757183_40757184delinsTC , CM000674.1:g.40757183_40757184delinsTC GRCh37
NC_000012.10:g.39043450_39043451delinsTC NCBI36
NG_011709.1:g.143371_143372delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.7029-21_7029-20delinsTC MANE Select ENSP00000298910.7:n.7029-21_7029-20delinsTC
ENST00000636518.1:c.826-21_826-20delinsTC
ENST00000679360.1:c.*5938-21_*5938-20delinsTC ENSP00000505368.1:n.*5938-21_*5938-20delinsTC
ENST00000679532.1:c.2803-21_2803-20delinsTC
ENST00000679683.1:c.819-21_819-20delinsTC
ENST00000680018.1:c.2474-21_2474-20delinsTC ENSP00000505347.1:n.2474-21_2474-20delinsTC
ENST00000680422.1:c.4116-21_4116-20delinsTC
ENST00000680425.1:c.2196-21_2196-20delinsTC ENSP00000506459.1:n.2196-21_2196-20delinsTC
ENST00000680453.1:c.2486-21_2486-20delinsTC
ENST00000680790.1:c.6774-21_6774-20delinsTC ENSP00000505335.1:n.6774-21_6774-20delinsTC
ENST00000681136.1:n.3013-21_3013-20delinsTC
ENST00000681696.1:c.2712-21_2712-20delinsTC ENSP00000505871.1:n.2712-21_2712-20delinsTC
ENST00000681773.1:n.236-21_236-20delinsTC
ENST00000298910.11:c.7029-21_7029-20delinsTC ENSP00000298910.7:n.7029-21_7029-20delinsTC
ENST00000430804.5:c.4325-21_4325-20delinsTC
ENST00000479187.5:n.3710-21_3710-20delinsTC
NM_198578.3:c.7029-21_7029-20delinsTC NP_940980.3:n.7029-21_7029-20delinsTC
XM_005268629.2:c.7029-21_7029-20delinsTC XP_005268686.1:n.7029-21_7029-20delinsTC
XM_011537877.1:c.7029-21_7029-20delinsTC XP_011536179.1:n.7029-21_7029-20delinsTC
XM_011537879.1:c.5826-21_5826-20delinsTC XP_011536181.1:n.5826-21_5826-20delinsTC
XR_944868.1:n.485-8555_485-8554delinsGA
XM_005268629.4:c.7029-21_7029-20delinsTC XP_005268686.1:n.7029-21_7029-20delinsTC
XM_011537877.3:c.7029-21_7029-20delinsTC XP_011536179.1:n.7029-21_7029-20delinsTC
XM_017018787.1:c.3945-21_3945-20delinsTC XP_016874276.1:n.3945-21_3945-20delinsTC
XM_017018788.2:c.3291-21_3291-20delinsTC XP_016874277.1:n.3291-21_3291-20delinsTC
XM_024448833.1:c.5826-21_5826-20delinsTC XP_024304601.1:n.5826-21_5826-20delinsTC
XR_944868.2:n.485-8555_485-8554delinsGA
NM_198578.4:c.7029-21_7029-20delinsTC MANE Select NP_940980.4:n.7029-21_7029-20delinsTC