Canonical Allele Identifier: CA384417994
Gene: LRRK2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40309121A>T , CM000674.2:g.40309121A>T GRCh38
NC_000012.11:g.40702923A>T , CM000674.1:g.40702923A>T GRCh37
NC_000012.10:g.38989190A>T NCBI36
NG_011709.1:g.89111A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000298910.12:c.4205A>T MANE Select ENSP00000298910.7:p.Tyr1402Phe
ENST00000679360.1:c.*3114A>T ENSP00000505368.1:n.*3114A>T
ENST00000680790.1:c.3950A>T ENSP00000505335.1:p.Tyr1317Phe
ENST00000298910.11:c.4205A>T ENSP00000298910.7:p.Tyr1402Phe
ENST00000430804.5:c.1501A>T
ENST00000479187.5:n.886A>T
NM_198578.3:c.4205A>T NP_940980.3:p.Tyr1402Phe
XM_005268629.2:c.4205A>T XP_005268686.1:p.Tyr1402Phe
XM_011537877.1:c.4205A>T XP_011536179.1:p.Tyr1402Phe
XM_011537878.1:c.4205A>T XP_011536180.1:p.Tyr1402Phe
XM_011537879.1:c.3002A>T XP_011536181.1:p.Tyr1001Phe
XM_011537880.1:c.4205A>T XP_011536182.1:p.Tyr1402Phe
XM_011537881.1:c.4205A>T XP_011536183.1:p.Tyr1402Phe
XM_005268629.4:c.4205A>T XP_005268686.1:p.Tyr1402Phe
XM_011537877.3:c.4205A>T XP_011536179.1:p.Tyr1402Phe
XM_011537881.3:c.4205A>T XP_011536183.1:p.Tyr1402Phe
XM_017018786.2:c.4205A>T XP_016874275.1:p.Tyr1402Phe
XM_017018787.1:c.1121A>T XP_016874276.1:p.Tyr374Phe
XM_017018788.2:c.467A>T XP_016874277.1:p.Tyr156Phe
XM_024448833.1:c.3002A>T XP_024304601.1:p.Tyr1001Phe
XR_001748574.2:n.4447A>T
NM_198578.4:c.4205A>T MANE Select NP_940980.4:p.Tyr1402Phe