LDH info

Canonical Allele Identifier: CA163452
Gene: GPX4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 140615
ClinVar RCV Id: RCV000128831
dbSNP Id: rs775146234

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1105814G>A , CM000681.2:g.1105814G>A GRCh38
NC_000019.9:g.1105813G>A , CM000681.1:g.1105813G>A GRCh37
NC_000019.8:g.1056813G>A NCBI36
NG_050621.1:g.6889G>A

Transcript Alleles

HGVS Amino-acid change
NM_001039847.2:c.476+5G>A VV NP_001034936.1:p.=
NM_001039848.2:c.587+5G>A VV NP_001034937.1:p.=
NM_002085.4:c.476+5G>A VV NP_002076.2:p.=
NM_001039848.3:c.587+5G>A VV NP_001034937.1:p.=
NM_001039847.3:c.476+5G>A VV NP_001034936.1:p.=
NM_001039848.4:c.587+5G>A VV NP_001034937.1:p.=
NM_001367832.1:c.395+5G>A VV NP_001354761.1:p.=
NM_002085.5:c.476+5G>A VV MANE Preferred NP_002076.2:p.=
ENST00000354171.12:c.476+5G>A ENSP00000346103.7:p.=
ENST00000585480.1:n.209+5G>A ENSP00000467900.1:p.=
ENST00000587648.5:c.356+5G>A ENSP00000468349.1:p.=
ENST00000588919.5:c.395+5G>A ENSP00000464989.3:p.=
ENST00000589115.5:c.476+5G>A ENSP00000466872.2:p.=
ENST00000592940.2:n.420G>A
ENST00000593032.5:c.395+5G>A ENSP00000465828.3:p.=
ENST00000611653.4:c.395+5G>A ENSP00000483655.1:p.=
ENST00000616066.4:c.473+5G>A ENSP00000485000.1:p.=
ENST00000622390.4:c.584+5G>A ENSP00000477503.1:p.=