LDH info

Canonical Allele Identifier: CA384404028
Gene: LRRK2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340414C>G , CM000674.2:g.40340414C>G GRCh38
NC_000012.11:g.40734216C>G , CM000674.1:g.40734216C>G GRCh37
NC_000012.10:g.39020483C>G NCBI36
NG_011709.1:g.120404C>G

Transcript Alleles

HGVS Amino-acid change
NM_198578.3:c.6069C>G VV NP_940980.3:p.Tyr2023Ter
XM_005268629.2:c.6069C>G XP_005268686.1:p.Tyr2023Ter
XM_011537877.1:c.6069C>G XP_011536179.1:p.Tyr2023Ter
XM_011537878.1:c.6069C>G XP_011536180.1:p.Tyr2023Ter
XM_011537879.1:c.4866C>G XP_011536181.1:p.Tyr1622Ter
XM_005268629.4:c.6069C>G XP_005268686.1:p.Tyr2023Ter
XM_011537877.3:c.6069C>G XP_011536179.1:p.Tyr2023Ter
XM_017018787.1:c.2985C>G XP_016874276.1:p.Tyr995Ter
XM_017018788.2:c.2331C>G XP_016874277.1:p.Tyr777Ter
XM_024448833.1:c.4866C>G XP_024304601.1:p.Tyr1622Ter
NM_198578.4:c.6069C>G VV MANE Preferred NP_940980.4:p.Tyr2023Ter
ENST00000298910.11:c.6069C>G ENSP00000298910.7:p.Tyr2023Ter
ENST00000430804.5:n.3365C>G
ENST00000479187.5:n.2750C>G