LDH info

Canonical Allele Identifier: CA384404023
Gene: LRRK2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340412T>G , CM000674.2:g.40340412T>G GRCh38
NC_000012.11:g.40734214T>G , CM000674.1:g.40734214T>G GRCh37
NC_000012.10:g.39020481T>G NCBI36
NG_011709.1:g.120402T>G

Transcript Alleles

HGVS Amino-acid change
NM_198578.3:c.6067T>G VV NP_940980.3:p.Tyr2023Asp
XM_005268629.2:c.6067T>G XP_005268686.1:p.Tyr2023Asp
XM_011537877.1:c.6067T>G XP_011536179.1:p.Tyr2023Asp
XM_011537878.1:c.6067T>G XP_011536180.1:p.Tyr2023Asp
XM_011537879.1:c.4864T>G XP_011536181.1:p.Tyr1622Asp
XM_005268629.4:c.6067T>G XP_005268686.1:p.Tyr2023Asp
XM_011537877.3:c.6067T>G XP_011536179.1:p.Tyr2023Asp
XM_017018787.1:c.2983T>G XP_016874276.1:p.Tyr995Asp
XM_017018788.2:c.2329T>G XP_016874277.1:p.Tyr777Asp
XM_024448833.1:c.4864T>G XP_024304601.1:p.Tyr1622Asp
NM_198578.4:c.6067T>G VV MANE Preferred NP_940980.4:p.Tyr2023Asp
ENST00000298910.11:c.6067T>G ENSP00000298910.7:p.Tyr2023Asp
ENST00000430804.5:n.3363T>G
ENST00000479187.5:n.2748T>G