LDH info

Canonical Allele Identifier: CA9037128
Gene: GPX4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs4807542

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1104079G>A , CM000681.2:g.1104079G>A GRCh38
NC_000019.9:g.1104078G>A , CM000681.1:g.1104078G>A GRCh37
NC_000019.8:g.1055078G>A NCBI36
NG_050621.1:g.5154G>A

Transcript Alleles

HGVS Amino-acid change
NM_001039847.2:c.36G>A VV NP_001034936.1:p.Pro12=
NM_002085.4:c.36G>A VV NP_002076.2:p.Pro12=
NM_001039847.3:c.36G>A VV NP_001034936.1:p.Pro12=
NM_001367832.1:c.-46G>A VV NP_001354761.1:p.=
NM_002085.5:c.36G>A VV MANE Preferred NP_002076.2:p.Pro12=
ENST00000354171.12:c.36G>A ENSP00000346103.7:p.Pro12=
ENST00000588919.5:c.-46G>A ENSP00000464989.3:p.=
ENST00000589115.5:c.36G>A ENSP00000466872.2:p.Pro12=
ENST00000593032.5:c.-46G>A ENSP00000465828.3:p.=
ENST00000611653.4:c.-46G>A ENSP00000483655.1:p.=
ENST00000616066.4:c.36G>A ENSP00000485000.1:p.Pro12=