LDH info

Canonical Allele Identifier: CA219309
Gene: SLC37A4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6923
dbSNP Id: rs80356489

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119028223A>G , CM000673.2:g.119028223A>G GRCh38
NC_000011.9:g.118898933A>G , CM000673.1:g.118898933A>G GRCh37
NC_000011.8:g.118404143A>G NCBI36
NG_013331.1:g.7684T>C , LRG_187:g.7684T>C

Transcript Alleles

HGVS Amino-acid change
NM_001164277.1:c.352T>C , LRG_187t1:c.352T>C NP_001157749.1:p.Trp118Arg
NM_001164278.1:c.352T>C VV NP_001157750.1:p.Trp118Arg
NM_001164279.1:c.133T>C VV NP_001157751.1:p.Trp45Arg
NM_001164280.1:c.352T>C VV NP_001157752.1:p.Trp118Arg
NM_001467.5:c.352T>C VV NP_001458.1:p.Trp118Arg
NM_001164278.2:c.352T>C VV NP_001157750.1:p.Trp118Arg
NM_001164279.2:c.133T>C VV NP_001157751.1:p.Trp45Arg
NM_001164280.2:c.352T>C VV NP_001157752.1:p.Trp118Arg
NM_001467.6:c.352T>C VV NP_001458.1:p.Trp118Arg
ENST00000330775.9:c.352T>C ENSP00000476242.2:p.Trp118Arg
ENST00000357590.9:c.352T>C ENSP00000476176.2:p.Trp118Arg
ENST00000524428.5:n.352T>C
ENST00000525039.5:n.775T>C
ENST00000525102.5:n.1109T>C
ENST00000525372.5:n.352T>C
ENST00000525787.1:n.647T>C
ENST00000526275.5:n.812T>C
ENST00000526626.6:n.344-351T>C
ENST00000527992.5:n.579T>C
ENST00000529510.5:n.370T>C
ENST00000530407.5:n.501T>C
ENST00000532085.1:n.2641T>C
ENST00000532888.6:n.647T>C
ENST00000538950.5:c.133T>C ENSP00000475991.2:p.Trp45Arg
ENST00000545985.5:c.352T>C ENSP00000475241.2:p.Trp118Arg