Canonical Allele Identifier: CA2031026036
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363529C= , CM000674.2:g.40363529C= GRCh38
NC_000012.11:g.40757331C= , CM000674.1:g.40757331C= GRCh37
NC_000012.10:g.39043598C= NCBI36
NG_011709.1:g.143519C=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7156C= MANE Select ENSP00000298910.7:p.Leu2386=
ENST00000636518.1:c.953C=
ENST00000679360.1:c.*6065C= ENSP00000505368.1:n.*6065C=
ENST00000679532.1:c.2930C=
ENST00000679683.1:c.946C=
ENST00000680018.1:c.2601C= ENSP00000505347.1:n.2601C=
ENST00000680422.1:c.4243C=
ENST00000680425.1:c.2323C= ENSP00000506459.1:n.2323C=
ENST00000680453.1:c.2613C=
ENST00000680790.1:c.6901C= ENSP00000505335.1:p.Leu2301=
ENST00000681136.1:n.3140C=
ENST00000681696.1:c.2839C= ENSP00000505871.1:p.Leu947=
ENST00000681773.1:n.363C=
ENST00000298910.11:c.7156C= ENSP00000298910.7:p.Leu2386=
ENST00000430804.5:c.4452C=
ENST00000479187.5:n.3837C=
NM_198578.3:c.7156C= NP_940980.3:p.Leu2386=
XM_005268629.2:c.7156C= XP_005268686.1:p.Leu2386=
XM_011537877.1:c.7156C= XP_011536179.1:p.Leu2386=
XM_011537879.1:c.5953C= XP_011536181.1:p.Leu1985=
XR_944868.1:n.485-8702G=
XM_005268629.4:c.7156C= XP_005268686.1:p.Leu2386=
XM_011537877.3:c.7156C= XP_011536179.1:p.Leu2386=
XM_017018787.1:c.4072C= XP_016874276.1:p.Leu1358=
XM_017018788.2:c.3418C= XP_016874277.1:p.Leu1140=
XM_024448833.1:c.5953C= XP_024304601.1:p.Leu1985=
XR_944868.2:n.485-8702G=
NM_198578.4:c.7156C= MANE Select NP_940980.4:p.Leu2386=