LDH info

Canonical Allele Identifier: CA64882686
Gene: METTL21A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7569963

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.207608460G>A , CM000664.2:g.207608460G>A GRCh38
NC_000002.11:g.208473184G>A , CM000664.1:g.208473184G>A GRCh37
NC_000002.10:g.208181429G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001308021.1:c.259+13346C>T VV NP_001294950.1:p.=
XM_011510727.1:c.334+13346C>T XP_011509029.1:p.=
XM_011510728.1:c.334+13346C>T XP_011509030.1:p.=
XM_011510729.1:c.388+12181C>T XP_011509031.1:p.=
NM_001308021.2:c.259+13346C>T VV NP_001294950.1:p.=
NM_001330131.1:c.259+13346C>T VV NP_001317060.1:p.=
NM_001330132.1:c.259+13346C>T VV NP_001317061.1:p.=
NM_001330133.1:c.259+13346C>T VV NP_001317062.1:p.=
NM_001330135.1:c.259+13346C>T VV NP_001317064.1:p.=
NM_001330136.1:c.259+13346C>T VV NP_001317065.1:p.=
XM_011510727.3:c.334+13346C>T XP_011509029.1:p.=
XM_011510728.3:c.334+13346C>T XP_011509030.1:p.=
XM_011510729.2:c.388+12181C>T XP_011509031.1:p.=
XM_017003445.1:c.334+13346C>T XP_016858934.1:p.=
XM_024452724.1:c.259+13346C>T XP_024308492.1:p.=
XM_024452725.1:c.259+13346C>T XP_024308493.1:p.=
XM_024452726.1:c.313+12181C>T XP_024308494.1:p.=
NM_001308021.3:c.259+13346C>T VV NP_001294950.1:p.=
NM_001330131.2:c.259+13346C>T VV NP_001317060.1:p.=
NM_001330135.2:c.259+13346C>T VV NP_001317064.1:p.=
ENST00000425132.5:c.259+13346C>T ENSP00000400730.1:p.=
ENST00000432416.5:c.259+13346C>T ENSP00000416570.1:p.=
ENST00000458426.5:c.259+13346C>T ENSP00000389684.1:p.=