Canonical Allele Identifier: CA2031025527
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363330_40363331delinsAG , CM000674.2:g.40363330_40363331delinsAG GRCh38
NC_000012.11:g.40757132_40757133delinsAG , CM000674.1:g.40757132_40757133delinsAG GRCh37
NC_000012.10:g.39043399_39043400delinsAG NCBI36
NG_011709.1:g.143320_143321delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.7029-72_7029-71delinsAG MANE Select ENSP00000298910.7:n.7029-72_7029-71delinsAG
ENST00000636518.1:c.826-72_826-71delinsAG
ENST00000679360.1:c.*5938-72_*5938-71delinsAG ENSP00000505368.1:n.*5938-72_*5938-71delinsAG
ENST00000679532.1:c.2803-72_2803-71delinsAG
ENST00000679683.1:c.819-72_819-71delinsAG
ENST00000680018.1:c.2474-72_2474-71delinsAG ENSP00000505347.1:n.2474-72_2474-71delinsAG
ENST00000680422.1:c.4116-72_4116-71delinsAG
ENST00000680425.1:c.2196-72_2196-71delinsAG ENSP00000506459.1:n.2196-72_2196-71delinsAG
ENST00000680453.1:c.2486-72_2486-71delinsAG
ENST00000680790.1:c.6774-72_6774-71delinsAG ENSP00000505335.1:n.6774-72_6774-71delinsAG
ENST00000681136.1:n.3013-72_3013-71delinsAG
ENST00000681696.1:c.2712-72_2712-71delinsAG ENSP00000505871.1:n.2712-72_2712-71delinsAG
ENST00000681773.1:n.236-72_236-71delinsAG
ENST00000298910.11:c.7029-72_7029-71delinsAG ENSP00000298910.7:n.7029-72_7029-71delinsAG
ENST00000430804.5:c.4325-72_4325-71delinsAG
ENST00000479187.5:n.3710-72_3710-71delinsAG
NM_198578.3:c.7029-72_7029-71delinsAG NP_940980.3:n.7029-72_7029-71delinsAG
XM_005268629.2:c.7029-72_7029-71delinsAG XP_005268686.1:n.7029-72_7029-71delinsAG
XM_011537877.1:c.7029-72_7029-71delinsAG XP_011536179.1:n.7029-72_7029-71delinsAG
XM_011537879.1:c.5826-72_5826-71delinsAG XP_011536181.1:n.5826-72_5826-71delinsAG
XR_944868.1:n.485-8504_485-8503delinsCT
XM_005268629.4:c.7029-72_7029-71delinsAG XP_005268686.1:n.7029-72_7029-71delinsAG
XM_011537877.3:c.7029-72_7029-71delinsAG XP_011536179.1:n.7029-72_7029-71delinsAG
XM_017018787.1:c.3945-72_3945-71delinsAG XP_016874276.1:n.3945-72_3945-71delinsAG
XM_017018788.2:c.3291-72_3291-71delinsAG XP_016874277.1:n.3291-72_3291-71delinsAG
XM_024448833.1:c.5826-72_5826-71delinsAG XP_024304601.1:n.5826-72_5826-71delinsAG
XR_944868.2:n.485-8504_485-8503delinsCT
NM_198578.4:c.7029-72_7029-71delinsAG MANE Select NP_940980.4:n.7029-72_7029-71delinsAG