Canonical Allele Identifier: CA2031002718
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40309136A= , CM000674.2:g.40309136A= GRCh38
NC_000012.11:g.40702938A= , CM000674.1:g.40702938A= GRCh37
NC_000012.10:g.38989205A= NCBI36
NG_011709.1:g.89126A=

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.4220A= MANE Select ENSP00000298910.7:p.His1407=
ENST00000679360.1:c.*3129A= ENSP00000505368.1:n.*3129A=
ENST00000680790.1:c.3965A= ENSP00000505335.1:p.His1322=
ENST00000298910.11:c.4220A= ENSP00000298910.7:p.His1407=
ENST00000430804.5:c.1516A=
ENST00000479187.5:n.901A=
NM_198578.3:c.4220A= NP_940980.3:p.His1407=
XM_005268629.2:c.4220A= XP_005268686.1:p.His1407=
XM_011537877.1:c.4220A= XP_011536179.1:p.His1407=
XM_011537878.1:c.4220A= XP_011536180.1:p.His1407=
XM_011537879.1:c.3017A= XP_011536181.1:p.His1006=
XM_011537880.1:c.4220A= XP_011536182.1:p.His1407=
XM_011537881.1:c.4220A= XP_011536183.1:p.His1407=
XM_005268629.4:c.4220A= XP_005268686.1:p.His1407=
XM_011537877.3:c.4220A= XP_011536179.1:p.His1407=
XM_011537881.3:c.4220A= XP_011536183.1:p.His1407=
XM_017018786.2:c.4220A= XP_016874275.1:p.His1407=
XM_017018787.1:c.1136A= XP_016874276.1:p.His379=
XM_017018788.2:c.482A= XP_016874277.1:p.His161=
XM_024448833.1:c.3017A= XP_024304601.1:p.His1006=
XR_001748574.2:n.4462A=
NM_198578.4:c.4220A= MANE Select NP_940980.4:p.His1407=