Canonical Allele Identifier: CA359719774
Gene: NDUFS4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.52942175G>A (hg19) chr5:g.53646345G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53646345G>A , CM000667.2:g.53646345G>A GRCh38
NC_000005.9:g.52942175G>A , CM000667.1:g.52942175G>A GRCh37
NC_000005.8:g.52977932G>A NCBI36
NG_008200.1:g.90711G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000296684.10:c.290G>A MANE Select ENSP00000296684.5:p.Trp97Ter
ENST00000296684.9:c.290G>A ENSP00000296684.5:p.Trp97Ter
ENST00000502423.5:c.*157G>A ENSP00000422177.1:n.*157G>A
ENST00000506765.1:c.278G>A ENSP00000424570.1:p.Trp93Ter
ENST00000506974.5:c.*66G>A ENSP00000425967.1:n.*66G>A
ENST00000507026.5:c.*264G>A ENSP00000424993.1:n.*264G>A
ENST00000509443.1:n.151G>A
NM_002495.2:c.290G>A NP_002486.1:p.Trp97Ter
XM_005248525.3:c.290G>A XP_005248582.1:p.Trp97Ter
XM_011543415.1:c.116G>A XP_011541717.1:p.Trp39Ter
NM_001318051.1:c.290G>A NP_001304980.1:p.Trp97Ter
NM_002495.3:c.290G>A NP_002486.1:p.Trp97Ter
NR_134473.1:n.492G>A
NR_134474.1:n.409G>A
NR_134475.1:n.444G>A
NM_002495.4:c.290G>A MANE Select NP_002486.1:p.Trp97Ter
NM_001318051.2:c.290G>A NP_001304980.1:p.Trp97Ter
NR_134473.2:n.486G>A
NR_134474.2:n.403G>A
NR_134475.2:n.438G>A
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