Canonical Allele Identifier: CA2030983035

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298787_40298806delinsATATATATATATAATATATG , CM000674.2:g.40298787_40298806delinsATATATATATATAATATATG	GRCh38
NC_000012.11:g.40692589_40692608delinsATATATATATATAATATATG , CM000674.1:g.40692589_40692608delinsATATATATATATAATATATG	GRCh37
NC_000012.10:g.38978856_38978875delinsATATATATATATAATATATG	NCBI36
NG_011709.1:g.78777_78796delinsATATATATATATAATATATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3347+294_3348-303delinsATATATATATATAATATATG MANE Select	ENSP00000298910.7:n.3347+294_3348-303delinsATATATATATATAATATA...
ENST00000679360.1:c.*2256+294_*2257-303delinsATATATATATATAATATATG	ENSP00000505368.1:n.*2256+294_*2257-303delinsATATATATATATAATA...
ENST00000680790.1:c.3092+294_3093-303delinsATATATATATATAATATATG	ENSP00000505335.1:n.3092+294_3093-303delinsATATATATATATAATATA...
ENST00000298910.11:c.3347+294_3348-303delinsATATATATATATAATATATG	ENSP00000298910.7:n.3347+294_3348-303delinsATATATATATATAATATA...
ENST00000343742.6:c.3347+294_3348-303delinsATATATATATATAATATATG	ENSP00000341930.2:n.3347+294_3348-303delinsATATATATATATAATATA...
ENST00000430804.5:c.391+294_392-303delinsATATATATATATAATATATG
ENST00000479187.5:n.28+294_29-303delinsATATATATATATAATATATG
NM_198578.3:c.3347+294_3348-303delinsATATATATATATAATATATG	NP_940980.3:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_005268629.2:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_005268686.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537877.1:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536179.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537878.1:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536180.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537879.1:c.2144+294_2145-303delinsATATATATATATAATATATG	XP_011536181.1:n.2144+294_2145-303delinsATATATATATATAATATATG
XM_011537880.1:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536182.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537881.1:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536183.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537882.1:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536184.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_005268629.4:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_005268686.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537877.3:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536179.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537881.3:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536183.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_011537882.3:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_011536184.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_017018786.2:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_016874275.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_017018787.1:c.263+294_264-303delinsATATATATATATAATATATG	XP_016874276.1:n.263+294_264-303delinsATATATATATATAATATATG
XM_017018789.2:c.3347+294_3348-303delinsATATATATATATAATATATG	XP_016874278.1:n.3347+294_3348-303delinsATATATATATATAATATATG
XM_024448833.1:c.2144+294_2145-303delinsATATATATATATAATATATG	XP_024304601.1:n.2144+294_2145-303delinsATATATATATATAATATATG
XR_001748574.2:n.3589+294_3590-303delinsATATATATATATAATATATG
NM_198578.4:c.3347+294_3348-303delinsATATATATATATAATATATG MANE Select	NP_940980.4:n.3347+294_3348-303delinsATATATATATATAATATATG