LDH info

Canonical Allele Identifier: CA384404000
Gene: LRRK2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340407C>A , CM000674.2:g.40340407C>A GRCh38
NC_000012.11:g.40734209C>A , CM000674.1:g.40734209C>A GRCh37
NC_000012.10:g.39020476C>A NCBI36
NG_011709.1:g.120397C>A

Transcript Alleles

HGVS Amino-acid change
NM_198578.3:c.6062C>A VV NP_940980.3:p.Ala2021Asp
XM_005268629.2:c.6062C>A XP_005268686.1:p.Ala2021Asp
XM_011537877.1:c.6062C>A XP_011536179.1:p.Ala2021Asp
XM_011537878.1:c.6062C>A XP_011536180.1:p.Ala2021Asp
XM_011537879.1:c.4859C>A XP_011536181.1:p.Ala1620Asp
XM_005268629.4:c.6062C>A XP_005268686.1:p.Ala2021Asp
XM_011537877.3:c.6062C>A XP_011536179.1:p.Ala2021Asp
XM_017018787.1:c.2978C>A XP_016874276.1:p.Ala993Asp
XM_017018788.2:c.2324C>A XP_016874277.1:p.Ala775Asp
XM_024448833.1:c.4859C>A XP_024304601.1:p.Ala1620Asp
NM_198578.4:c.6062C>A VV MANE Preferred NP_940980.4:p.Ala2021Asp
ENST00000298910.11:c.6062C>A ENSP00000298910.7:p.Ala2021Asp
ENST00000430804.5:n.3358C>A
ENST00000479187.5:n.2743C>A