Canonical Allele Identifier: CA479238366
Gene: LRRK2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.40734102C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340300C>A , CM000674.2:g.40340300C>A GRCh38
NC_000012.11:g.40734102C>A , CM000674.1:g.40734102C>A GRCh37
NC_000012.10:g.39020369C>A NCBI36
NG_011709.1:g.120290C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.5955C>A MANE Select ENSP00000298910.7:p.Leu1985=
ENST00000679360.1:c.*4864C>A ENSP00000505368.1:n.*4864C>A
ENST00000679532.1:c.1729C>A
ENST00000680018.1:c.1400C>A ENSP00000505347.1:n.1400C>A
ENST00000680422.1:c.1600C>A
ENST00000680425.1:c.1122C>A ENSP00000506459.1:n.1122C>A
ENST00000680453.1:c.1412C>A
ENST00000680790.1:c.5700C>A ENSP00000505335.1:p.Leu1900=
ENST00000681136.1:n.1939C>A
ENST00000681696.1:c.1638C>A ENSP00000505871.1:p.Leu546=
ENST00000298910.11:c.5955C>A ENSP00000298910.7:p.Leu1985=
ENST00000430804.5:c.3251C>A
ENST00000479187.5:n.2636C>A
NM_198578.3:c.5955C>A NP_940980.3:p.Leu1985=
XM_005268629.2:c.5955C>A XP_005268686.1:p.Leu1985=
XM_011537877.1:c.5955C>A XP_011536179.1:p.Leu1985=
XM_011537878.1:c.5955C>A XP_011536180.1:p.Leu1985=
XM_011537879.1:c.4752C>A XP_011536181.1:p.Leu1584=
XM_005268629.4:c.5955C>A XP_005268686.1:p.Leu1985=
XM_011537877.3:c.5955C>A XP_011536179.1:p.Leu1985=
XM_017018787.1:c.2871C>A XP_016874276.1:p.Leu957=
XM_017018788.2:c.2217C>A XP_016874277.1:p.Leu739=
XM_024448833.1:c.4752C>A XP_024304601.1:p.Leu1584=
NM_198578.4:c.5955C>A MANE Select NP_940980.4:p.Leu1985=