Canonical Allele Identifier: CA2031000100
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40351568_40351572delinsAGTCT , CM000674.2:g.40351568_40351572delinsAGTCT GRCh38
NC_000012.11:g.40745370_40745374delinsAGTCT , CM000674.1:g.40745370_40745374delinsAGTCT GRCh37
NC_000012.10:g.39031637_39031641delinsAGTCT NCBI36
NG_011709.1:g.131558_131562delinsAGTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.6411_6415delinsAGTCT MANE Select ENSP00000298910.7:p.Leu2137=
ENST00000636518.1:c.208_212delinsAGTCT
ENST00000679360.1:c.*5320_*5324delinsAGTCT ENSP00000505368.1:n.*5320_*5324delinsAGTCT
ENST00000679532.1:c.2185_2189delinsAGTCT
ENST00000679683.1:c.201_205delinsAGTCT
ENST00000680018.1:c.1856_1860delinsAGTCT ENSP00000505347.1:n.1856_1860delinsAGTCT
ENST00000680422.1:c.2056_2060delinsAGTCT
ENST00000680425.1:c.1578_1582delinsAGTCT ENSP00000506459.1:n.1578_1582delinsAGTCT
ENST00000680453.1:c.1868_1872delinsAGTCT
ENST00000680790.1:c.6156_6160delinsAGTCT ENSP00000505335.1:p.Leu2052=
ENST00000681136.1:n.2395_2399delinsAGTCT
ENST00000681696.1:c.2094_2098delinsAGTCT ENSP00000505871.1:p.Leu698=
ENST00000298910.11:c.6411_6415delinsAGTCT ENSP00000298910.7:p.Leu2137=
ENST00000430804.5:c.3707_3711delinsAGTCT
ENST00000479187.5:n.3092_3096delinsAGTCT
NM_198578.3:c.6411_6415delinsAGTCT NP_940980.3:p.Leu2137=
XM_005268629.2:c.6411_6415delinsAGTCT XP_005268686.1:p.Leu2137=
XM_011537877.1:c.6411_6415delinsAGTCT XP_011536179.1:p.Leu2137=
XM_011537878.1:c.6411_6415delinsAGTCT XP_011536180.1:p.Leu2137=
XM_011537879.1:c.5208_5212delinsAGTCT XP_011536181.1:p.Leu1736=
XM_005268629.4:c.6411_6415delinsAGTCT XP_005268686.1:p.Leu2137=
XM_011537877.3:c.6411_6415delinsAGTCT XP_011536179.1:p.Leu2137=
XM_017018787.1:c.3327_3331delinsAGTCT XP_016874276.1:p.Leu1109=
XM_017018788.2:c.2673_2677delinsAGTCT XP_016874277.1:p.Leu891=
XM_024448833.1:c.5208_5212delinsAGTCT XP_024304601.1:p.Leu1736=
NM_198578.4:c.6411_6415delinsAGTCT MANE Select NP_940980.4:p.Leu2137=