Canonical Allele Identifier: CA2030983843

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40299110_40299112delinsAAT , CM000674.2:g.40299110_40299112delinsAAT	GRCh38
NC_000012.11:g.40692912_40692914delinsAAT , CM000674.1:g.40692912_40692914delinsAAT	GRCh37
NC_000012.10:g.38979179_38979181delinsAAT	NCBI36
NG_011709.1:g.79100_79102delinsAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.3349_3351delinsAAT MANE Select	ENSP00000298910.7:p.Asn1117=
ENST00000679360.1:c.*2258_*2260delinsAAT	ENSP00000505368.1:n.*2258_*2260delinsAAT
ENST00000680790.1:c.3094_3096delinsAAT	ENSP00000505335.1:p.Asn1032=
ENST00000298910.11:c.3349_3351delinsAAT	ENSP00000298910.7:p.Asn1117=
ENST00000343742.6:c.3349_3351delinsAAT	ENSP00000341930.2:p.Asn1117=
ENST00000430804.5:c.393_395delinsAAT
ENST00000479187.5:n.30_32delinsAAT
NM_198578.3:c.3349_3351delinsAAT	NP_940980.3:p.Asn1117=
XM_005268629.2:c.3349_3351delinsAAT	XP_005268686.1:p.Asn1117=
XM_011537877.1:c.3349_3351delinsAAT	XP_011536179.1:p.Asn1117=
XM_011537878.1:c.3349_3351delinsAAT	XP_011536180.1:p.Asn1117=
XM_011537879.1:c.2146_2148delinsAAT	XP_011536181.1:p.Asn716=
XM_011537880.1:c.3349_3351delinsAAT	XP_011536182.1:p.Asn1117=
XM_011537881.1:c.3349_3351delinsAAT	XP_011536183.1:p.Asn1117=
XM_011537882.1:c.3349_3351delinsAAT	XP_011536184.1:p.Asn1117=
XM_005268629.4:c.3349_3351delinsAAT	XP_005268686.1:p.Asn1117=
XM_011537877.3:c.3349_3351delinsAAT	XP_011536179.1:p.Asn1117=
XM_011537881.3:c.3349_3351delinsAAT	XP_011536183.1:p.Asn1117=
XM_011537882.3:c.3349_3351delinsAAT	XP_011536184.1:p.Asn1117=
XM_017018786.2:c.3349_3351delinsAAT	XP_016874275.1:p.Asn1117=
XM_017018787.1:c.265_267delinsAAT	XP_016874276.1:p.Asn89=
XM_017018789.2:c.3349_3351delinsAAT	XP_016874278.1:p.Asn1117=
XM_024448833.1:c.2146_2148delinsAAT	XP_024304601.1:p.Asn716=
XR_001748574.2:n.3591_3593delinsAAT
NM_198578.4:c.3349_3351delinsAAT MANE Select	NP_940980.4:p.Asn1117=