Canonical Allele Identifier: CA2030983001

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40298770_40298775delinsCTCAAA , CM000674.2:g.40298770_40298775delinsCTCAAA	GRCh38
NC_000012.11:g.40692572_40692577delinsCTCAAA , CM000674.1:g.40692572_40692577delinsCTCAAA	GRCh37
NC_000012.10:g.38978839_38978844delinsCTCAAA	NCBI36
NG_011709.1:g.78760_78765delinsCTCAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3347+277_3347+282delinsCTCAAA MANE Select	ENSP00000298910.7:n.3347+277_3347+282delinsCTCAAA
ENST00000679360.1:c.*2256+277_*2256+282delinsCTCAAA	ENSP00000505368.1:n.*2256+277_*2256+282delinsCTCAAA
ENST00000680790.1:c.3092+277_3092+282delinsCTCAAA	ENSP00000505335.1:n.3092+277_3092+282delinsCTCAAA
ENST00000298910.11:c.3347+277_3347+282delinsCTCAAA	ENSP00000298910.7:n.3347+277_3347+282delinsCTCAAA
ENST00000343742.6:c.3347+277_3347+282delinsCTCAAA	ENSP00000341930.2:n.3347+277_3347+282delinsCTCAAA
ENST00000430804.5:c.391+277_391+282delinsCTCAAA
ENST00000479187.5:n.28+277_28+282delinsCTCAAA
NM_198578.3:c.3347+277_3347+282delinsCTCAAA	NP_940980.3:n.3347+277_3347+282delinsCTCAAA
XM_005268629.2:c.3347+277_3347+282delinsCTCAAA	XP_005268686.1:n.3347+277_3347+282delinsCTCAAA
XM_011537877.1:c.3347+277_3347+282delinsCTCAAA	XP_011536179.1:n.3347+277_3347+282delinsCTCAAA
XM_011537878.1:c.3347+277_3347+282delinsCTCAAA	XP_011536180.1:n.3347+277_3347+282delinsCTCAAA
XM_011537879.1:c.2144+277_2144+282delinsCTCAAA	XP_011536181.1:n.2144+277_2144+282delinsCTCAAA
XM_011537880.1:c.3347+277_3347+282delinsCTCAAA	XP_011536182.1:n.3347+277_3347+282delinsCTCAAA
XM_011537881.1:c.3347+277_3347+282delinsCTCAAA	XP_011536183.1:n.3347+277_3347+282delinsCTCAAA
XM_011537882.1:c.3347+277_3347+282delinsCTCAAA	XP_011536184.1:n.3347+277_3347+282delinsCTCAAA
XM_005268629.4:c.3347+277_3347+282delinsCTCAAA	XP_005268686.1:n.3347+277_3347+282delinsCTCAAA
XM_011537877.3:c.3347+277_3347+282delinsCTCAAA	XP_011536179.1:n.3347+277_3347+282delinsCTCAAA
XM_011537881.3:c.3347+277_3347+282delinsCTCAAA	XP_011536183.1:n.3347+277_3347+282delinsCTCAAA
XM_011537882.3:c.3347+277_3347+282delinsCTCAAA	XP_011536184.1:n.3347+277_3347+282delinsCTCAAA
XM_017018786.2:c.3347+277_3347+282delinsCTCAAA	XP_016874275.1:n.3347+277_3347+282delinsCTCAAA
XM_017018787.1:c.263+277_263+282delinsCTCAAA	XP_016874276.1:n.263+277_263+282delinsCTCAAA
XM_017018789.2:c.3347+277_3347+282delinsCTCAAA	XP_016874278.1:n.3347+277_3347+282delinsCTCAAA
XM_024448833.1:c.2144+277_2144+282delinsCTCAAA	XP_024304601.1:n.2144+277_2144+282delinsCTCAAA
XR_001748574.2:n.3589+277_3589+282delinsCTCAAA
NM_198578.4:c.3347+277_3347+282delinsCTCAAA MANE Select	NP_940980.4:n.3347+277_3347+282delinsCTCAAA