Canonical Allele Identifier: CA2031002482
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40309043_40309044delinsTA , CM000674.2:g.40309043_40309044delinsTA GRCh38
NC_000012.11:g.40702845_40702846delinsTA , CM000674.1:g.40702845_40702846delinsTA GRCh37
NC_000012.10:g.38989112_38989113delinsTA NCBI36
NG_011709.1:g.89033_89034delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.4190-63_4190-62delinsTA MANE Select ENSP00000298910.7:n.4190-63_4190-62delins...
ENST00000679360.1:c.*3099-63_*3099-62delinsTA ENSP00000505368.1:n.*3099-63_*3099-62deli...
ENST00000680790.1:c.3935-63_3935-62delinsTA ENSP00000505335.1:n.3935-63_3935-62delins...
ENST00000298910.11:c.4190-63_4190-62delinsTA ENSP00000298910.7:n.4190-63_4190-62delins...
ENST00000430804.5:c.1486-63_1486-62delinsTA
ENST00000479187.5:n.871-63_871-62delinsTA
NM_198578.3:c.4190-63_4190-62delinsTA NP_940980.3:n.4190-63_4190-62delinsTA
XM_005268629.2:c.4190-63_4190-62delinsTA XP_005268686.1:n.4190-63_4190-62delinsTA
XM_011537877.1:c.4190-63_4190-62delinsTA XP_011536179.1:n.4190-63_4190-62delinsTA
XM_011537878.1:c.4190-63_4190-62delinsTA XP_011536180.1:n.4190-63_4190-62delinsTA
XM_011537879.1:c.2987-63_2987-62delinsTA XP_011536181.1:n.2987-63_2987-62delinsTA
XM_011537880.1:c.4190-63_4190-62delinsTA XP_011536182.1:n.4190-63_4190-62delinsTA
XM_011537881.1:c.4190-63_4190-62delinsTA XP_011536183.1:n.4190-63_4190-62delinsTA
XM_005268629.4:c.4190-63_4190-62delinsTA XP_005268686.1:n.4190-63_4190-62delinsTA
XM_011537877.3:c.4190-63_4190-62delinsTA XP_011536179.1:n.4190-63_4190-62delinsTA
XM_011537881.3:c.4190-63_4190-62delinsTA XP_011536183.1:n.4190-63_4190-62delinsTA
XM_017018786.2:c.4190-63_4190-62delinsTA XP_016874275.1:n.4190-63_4190-62delinsTA
XM_017018787.1:c.1106-63_1106-62delinsTA XP_016874276.1:n.1106-63_1106-62delinsTA
XM_017018788.2:c.452-63_452-62delinsTA XP_016874277.1:n.452-63_452-62delinsTA
XM_024448833.1:c.2987-63_2987-62delinsTA XP_024304601.1:n.2987-63_2987-62delinsTA
XR_001748574.2:n.4432-63_4432-62delinsTA
NM_198578.4:c.4190-63_4190-62delinsTA MANE Select NP_940980.4:n.4190-63_4190-62delinsTA