LDH info

Canonical Allele Identifier: CA384403989
Gene: LRRK2 HGNC NCBI

Identifiers and link-outs to other resources

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.40340403A>T , CM000674.2:g.40340403A>T GRCh38
NC_000012.11:g.40734205A>T , CM000674.1:g.40734205A>T GRCh37
NC_000012.10:g.39020472A>T NCBI36
NG_011709.1:g.120393A>T

Transcript Alleles

HGVS Amino-acid change
NM_198578.3:c.6058A>T VV NP_940980.3:p.Ile2020Phe
XM_005268629.2:c.6058A>T XP_005268686.1:p.Ile2020Phe
XM_011537877.1:c.6058A>T XP_011536179.1:p.Ile2020Phe
XM_011537878.1:c.6058A>T XP_011536180.1:p.Ile2020Phe
XM_011537879.1:c.4855A>T XP_011536181.1:p.Ile1619Phe
XM_005268629.4:c.6058A>T XP_005268686.1:p.Ile2020Phe
XM_011537877.3:c.6058A>T XP_011536179.1:p.Ile2020Phe
XM_017018787.1:c.2974A>T XP_016874276.1:p.Ile992Phe
XM_017018788.2:c.2320A>T XP_016874277.1:p.Ile774Phe
XM_024448833.1:c.4855A>T XP_024304601.1:p.Ile1619Phe
NM_198578.4:c.6058A>T VV MANE Preferred NP_940980.4:p.Ile2020Phe
ENST00000298910.11:c.6058A>T ENSP00000298910.7:p.Ile2020Phe
ENST00000430804.5:n.3354A>T
ENST00000479187.5:n.2739A>T