LDH info

Canonical Allele Identifier: CA273906
Gene: ACADM HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 188748
ClinVar RCV Id: RCV000169062
dbSNP Id: rs761317029

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75750449A>G , CM000663.2:g.75750449A>G GRCh38
NC_000001.10:g.76216134A>G , CM000663.1:g.76216134A>G GRCh37
NC_000001.9:g.75988722A>G NCBI36
NG_007045.2:g.31092A>G

Transcript Alleles

HGVS Amino-acid change
NM_000016.5:c.850-2A>G VV NP_000007.1:p.=
NM_001127328.2:c.862-2A>G VV NP_001120800.1:p.=
NM_001286042.1:c.742-2A>G VV NP_001272971.1:p.=
NM_001286043.1:c.949-2A>G VV NP_001272972.1:p.=
NM_001286044.1:c.283-2A>G VV NP_001272973.1:p.=
NM_000016.6:c.850-2A>G VV NP_000007.1:p.=
ENST00000370834.9:c.949-2A>G ENSP00000359871.5:p.=
ENST00000370841.8:c.850-2A>G ENSP00000359878.4:p.=
ENST00000420607.6:c.862-2A>G ENSP00000409612.2:p.=
ENST00000525808.5:c.*436-2A>G ENSP00000434823.1:p.=
ENST00000526129.5:c.*634-2A>G ENSP00000434092.1:p.=
ENST00000526196.5:c.*618-2A>G ENSP00000431953.1:p.=
ENST00000528016.1:n.64-2A>G ENSP00000434284.1:p.=
ENST00000529059.5:n.759-2A>G
ENST00000532207.5:n.580-2A>G
ENST00000534334.5:c.*434-2A>G ENSP00000435584.1:p.=
ENST00000541113.5:c.742-2A>G ENSP00000442324.1:p.=