LDH info

Canonical Allele Identifier: CA16040771
Gene: ACADM HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 370802
dbSNP Id: rs1057516778
COSMIC: COSM32206

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75724788A>G , CM000663.2:g.75724788A>G GRCh38
NC_000001.10:g.76190473A>G , CM000663.1:g.76190473A>G GRCh37
NC_000001.9:g.75963061A>G NCBI36
NG_007045.2:g.5431A>G

Transcript Alleles

HGVS Amino-acid change
NM_000016.5:c.1A>G VV
NM_001127328.2:c.1A>G VV
NM_001286042.1:c.-20A>G VV NP_001272971.1:p.=
NM_001286043.1:c.1A>G VV
NM_001286044.1:c.-297A>G VV NP_001272973.1:p.=
NM_000016.6:c.1A>G VV MANE Preferred
ENST00000370834.9:c.1A>G
ENST00000370841.8:c.1A>G
ENST00000420607.6:c.1A>G
ENST00000473018.2:n.34A>G
ENST00000525808.5:c.1A>G
ENST00000525881.5:n.98A>G
ENST00000526129.5:c.1A>G
ENST00000526196.5:c.1A>G
ENST00000530953.6:c.1A>G
ENST00000532509.5:c.1A>G
ENST00000534146.5:n.80A>G
ENST00000534334.5:c.1A>G
ENST00000541113.5:c.-20A>G ENSP00000442324.1:p.=