LDH info

Canonical Allele Identifier: CA219275
Gene: SLC37A4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6935
dbSNP Id: rs121908980

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.119025298C>T , CM000673.2:g.119025298C>T GRCh38
NC_000011.9:g.118896008C>T , CM000673.1:g.118896008C>T GRCh37
NC_000011.8:g.118401218C>T NCBI36
NG_013331.1:g.10608G>A , LRG_187:g.10608G>A

Transcript Alleles

HGVS Amino-acid change
NM_001164277.1:c.1016G>A , LRG_187t1:c.1016G>A NP_001157749.1:p.Gly339Asp
NM_001164278.1:c.1082G>A VV NP_001157750.1:p.Gly361Asp
NM_001164279.1:c.797G>A VV NP_001157751.1:p.Gly266Asp
NM_001164280.1:c.1016G>A VV NP_001157752.1:p.Gly339Asp
NM_001467.5:c.1016G>A VV NP_001458.1:p.Gly339Asp
NM_001164278.2:c.1082G>A VV NP_001157750.1:p.Gly361Asp
NM_001164279.2:c.797G>A VV NP_001157751.1:p.Gly266Asp
NM_001164280.2:c.1016G>A VV NP_001157752.1:p.Gly339Asp
NM_001467.6:c.1016G>A VV NP_001458.1:p.Gly339Asp
ENST00000330775.9:c.1016G>A ENSP00000476242.2:p.Gly339Asp
ENST00000357590.9:c.1082G>A ENSP00000476176.2:p.Gly361Asp
ENST00000524428.5:n.1252G>A
ENST00000525039.5:n.1506G>A
ENST00000525102.5:n.1774G>A
ENST00000525372.5:n.1114G>A
ENST00000526275.5:n.1798G>A
ENST00000527992.5:n.1244G>A
ENST00000529510.5:n.704G>A
ENST00000530407.5:n.1166G>A
ENST00000532085.1:n.5034G>A
ENST00000533058.5:c.*249C>T ENSP00000432920.1:p.=
ENST00000538950.5:c.797G>A ENSP00000475991.2:p.Gly266Asp
ENST00000545985.5:c.1016G>A ENSP00000475241.2:p.Gly339Asp