Canonical Allele Identifier: CA2031000265
Gene: LRRK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40351592A= , CM000674.2:g.40351592A= GRCh38
NC_000012.11:g.40745394A= , CM000674.1:g.40745394A= GRCh37
NC_000012.10:g.39031661A= NCBI36
NG_011709.1:g.131582A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000298910.12:c.6435A= MANE Select ENSP00000298910.7:p.Leu2145=
ENST00000636518.1:c.232A=
ENST00000679360.1:c.*5344A= ENSP00000505368.1:n.*5344A=
ENST00000679532.1:c.2209A=
ENST00000679683.1:c.225A=
ENST00000680018.1:c.1880A= ENSP00000505347.1:n.1880A=
ENST00000680422.1:c.2080A=
ENST00000680425.1:c.1602A= ENSP00000506459.1:n.1602A=
ENST00000680453.1:c.1892A=
ENST00000680790.1:c.6180A= ENSP00000505335.1:p.Leu2060=
ENST00000681136.1:n.2419A=
ENST00000681696.1:c.2118A= ENSP00000505871.1:p.Leu706=
ENST00000298910.11:c.6435A= ENSP00000298910.7:p.Leu2145=
ENST00000430804.5:c.3731A=
ENST00000479187.5:n.3116A=
NM_198578.3:c.6435A= NP_940980.3:p.Leu2145=
XM_005268629.2:c.6435A= XP_005268686.1:p.Leu2145=
XM_011537877.1:c.6435A= XP_011536179.1:p.Leu2145=
XM_011537878.1:c.6435A= XP_011536180.1:p.Leu2145=
XM_011537879.1:c.5232A= XP_011536181.1:p.Leu1744=
XM_005268629.4:c.6435A= XP_005268686.1:p.Leu2145=
XM_011537877.3:c.6435A= XP_011536179.1:p.Leu2145=
XM_017018787.1:c.3351A= XP_016874276.1:p.Leu1117=
XM_017018788.2:c.2697A= XP_016874277.1:p.Leu899=
XM_024448833.1:c.5232A= XP_024304601.1:p.Leu1744=
NM_198578.4:c.6435A= MANE Select NP_940980.4:p.Leu2145=