LDH info

Canonical Allele Identifier: CA15081236
Gene: ACADM HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs11161521

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750645T>C , CM000663.2:g.75750645T>C GRCh38
NC_000001.10:g.76216330T>C , CM000663.1:g.76216330T>C GRCh37
NC_000001.9:g.75988918T>C NCBI36
NG_007045.2:g.31288T>C

Transcript Alleles

HGVS Amino-acid change
NM_000016.5:c.945+99T>C VV NP_000007.1:p.=
NM_001127328.2:c.957+99T>C VV NP_001120800.1:p.=
NM_001286042.1:c.837+99T>C VV NP_001272971.1:p.=
NM_001286043.1:c.1044+99T>C VV NP_001272972.1:p.=
NM_001286044.1:c.378+99T>C VV NP_001272973.1:p.=
NM_000016.6:c.945+99T>C VV NP_000007.1:p.=
ENST00000370834.9:c.1044+99T>C ENSP00000359871.5:p.=
ENST00000370841.8:c.945+99T>C ENSP00000359878.4:p.=
ENST00000420607.6:c.957+99T>C ENSP00000409612.2:p.=
ENST00000481374.1:n.96+99T>C
ENST00000525808.5:c.*531+99T>C ENSP00000434823.1:p.=
ENST00000526129.5:c.*729+99T>C ENSP00000434092.1:p.=
ENST00000526196.5:c.*713+99T>C ENSP00000431953.1:p.=
ENST00000528016.1:n.159+99T>C ENSP00000434284.1:p.=
ENST00000529059.5:n.854+99T>C
ENST00000532207.5:n.675+99T>C
ENST00000534334.5:c.*529+99T>C ENSP00000435584.1:p.=
ENST00000541113.5:c.837+99T>C ENSP00000442324.1:p.=