LDH info

Canonical Allele Identifier: CA118550
Gene: NDUFS4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 6890
ClinVar RCV Id: RCV000007293
dbSNP Id: rs104893899

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53560706G>A , CM000667.2:g.53560706G>A GRCh38
NC_000005.9:g.52856536G>A , CM000667.1:g.52856536G>A GRCh37
NC_000005.8:g.52892293G>A NCBI36
NG_008200.1:g.5072G>A

Transcript Alleles

HGVS Amino-acid change
NM_002495.2:c.44G>A VV NP_002486.1:p.Trp15Ter
XM_005248525.3:c.44G>A XP_005248582.1:p.Trp15Ter
XM_011543414.1:c.44G>A XP_011541716.1:p.Trp15Ter
NM_001318051.1:c.44G>A VV NP_001304980.1:p.Trp15Ter
NM_002495.3:c.44G>A VV NP_002486.1:p.Trp15Ter
NR_134473.1:n.74G>A
NR_134474.1:n.74G>A
NR_134475.1:n.74G>A
XM_017009491.1:c.44G>A XP_016864980.1:p.Trp15Ter
NM_002495.4:c.44G>A VV MANE Preferred NP_002486.1:p.Trp15Ter
NM_001318051.2:c.44G>A VV NP_001304980.1:p.Trp15Ter
NR_134473.2:n.68G>A
NR_134474.2:n.68G>A
NR_134475.2:n.68G>A
ENST00000296684.9:c.44G>A ENSP00000296684.5:p.Trp15Ter
ENST00000502423.5:c.44G>A ENSP00000422177.1:p.Trp15Ter
ENST00000506765.1:n.32G>A ENSP00000424570.1:p.Trp11Ter
ENST00000506974.5:c.44G>A ENSP00000425967.1:p.Trp15Ter
ENST00000507026.5:c.44G>A ENSP00000424993.1:p.Trp15Ter