Canonical Allele Identifier: CA2843175471

Gene: LRRK2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.40253014dup , CM000674.2:g.40253014dup	GRCh38
NC_000012.11:g.40646816dup , CM000674.1:g.40646816dup	GRCh37
NC_000012.10:g.38933083dup	NCBI36
NG_011709.1:g.33004dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298910.12:c.1286dup MANE Select	ENSP00000298910.7:p.Asn429LysfsTer3
ENST00000679360.1:c.*195dup	ENSP00000505368.1:n.*195dup
ENST00000680790.1:c.1286dup	ENSP00000505335.1:p.Asn429LysfsTer16
ENST00000298910.11:c.1286dup	ENSP00000298910.7:p.Asn429LysfsTer3
ENST00000343742.6:c.1286dup	ENSP00000341930.2:p.Asn429LysfsTer3
ENST00000416796.5:c.660dup	ENSP00000398726.1:p.Cys221MetfsTer23
NM_198578.3:c.1286dup	NP_940980.3:p.Asn429LysfsTer3
XM_005268629.2:c.1286dup	XP_005268686.1:p.Asn429LysfsTer3
XM_011537877.1:c.1286dup	XP_011536179.1:p.Asn429LysfsTer3
XM_011537878.1:c.1286dup	XP_011536180.1:p.Asn429LysfsTer3
XM_011537879.1:c.83dup	XP_011536181.1:p.Asn28LysfsTer3
XM_011537880.1:c.1286dup	XP_011536182.1:p.Asn429LysfsTer3
XM_011537881.1:c.1286dup	XP_011536183.1:p.Asn429LysfsTer3
XM_011537882.1:c.1286dup	XP_011536184.1:p.Asn429LysfsTer3
XM_005268629.4:c.1286dup	XP_005268686.1:p.Asn429LysfsTer3
XM_011537877.3:c.1286dup	XP_011536179.1:p.Asn429LysfsTer3
XM_011537881.3:c.1286dup	XP_011536183.1:p.Asn429LysfsTer3
XM_011537882.3:c.1286dup	XP_011536184.1:p.Asn429LysfsTer3
XM_017018786.2:c.1286dup	XP_016874275.1:p.Asn429LysfsTer3
XM_017018789.2:c.1286dup	XP_016874278.1:p.Asn429LysfsTer3
XM_024448833.1:c.83dup	XP_024304601.1:p.Asn28LysfsTer3
XR_001748574.2:n.1528dup
NM_198578.4:c.1286dup MANE Select	NP_940980.4:p.Asn429LysfsTer3