Canonical Allele Identifier: CA6514856
Gene: LRRK2 HGNC NCBI

Linked Data

dbSNP Id: rs780498854

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40363540C>A , CM000674.2:g.40363540C>A GRCh38
NC_000012.11:g.40757342C>A , CM000674.1:g.40757342C>A GRCh37
NC_000012.10:g.39043609C>A NCBI36
NG_011709.1:g.143530C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.7167C>A MANE Select ENSP00000298910.7:p.Cys2389Ter
ENST00000636518.1:c.964C>A
ENST00000679360.1:c.*6076C>A ENSP00000505368.1:n.*6076C>A
ENST00000679532.1:c.2941C>A
ENST00000679683.1:c.957C>A
ENST00000680018.1:c.2612C>A ENSP00000505347.1:n.2612C>A
ENST00000680422.1:c.4254C>A
ENST00000680425.1:c.2334C>A ENSP00000506459.1:n.2334C>A
ENST00000680453.1:c.2624C>A
ENST00000680790.1:c.6912C>A ENSP00000505335.1:p.Cys2304Ter
ENST00000681136.1:n.3151C>A
ENST00000681696.1:c.2850C>A ENSP00000505871.1:p.Cys950Ter
ENST00000681773.1:n.374C>A
ENST00000298910.11:c.7167C>A ENSP00000298910.7:p.Cys2389Ter
ENST00000430804.5:c.4463C>A
ENST00000479187.5:n.3848C>A
NM_198578.3:c.7167C>A NP_940980.3:p.Cys2389Ter
XM_005268629.2:c.7167C>A XP_005268686.1:p.Cys2389Ter
XM_011537877.1:c.7167C>A XP_011536179.1:p.Cys2389Ter
XM_011537879.1:c.5964C>A XP_011536181.1:p.Cys1988Ter
XR_944868.1:n.485-8713G>T
XM_005268629.4:c.7167C>A XP_005268686.1:p.Cys2389Ter
XM_011537877.3:c.7167C>A XP_011536179.1:p.Cys2389Ter
XM_017018787.1:c.4083C>A XP_016874276.1:p.Cys1361Ter
XM_017018788.2:c.3429C>A XP_016874277.1:p.Cys1143Ter
XM_024448833.1:c.5964C>A XP_024304601.1:p.Cys1988Ter
XR_944868.2:n.485-8713G>T
NM_198578.4:c.7167C>A MANE Select NP_940980.4:p.Cys2389Ter