Canonical Allele Identifier: CA359719267

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52954452A>G (hg19) ; chr5:g.53658622A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658622A>G , CM000667.2:g.53658622A>G	GRCh38
NC_000005.9:g.52954452A>G , CM000667.1:g.52954452A>G	GRCh37
NC_000005.8:g.52990209A>G	NCBI36
NG_008200.1:g.102988A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.422A>G MANE Select	ENSP00000296684.5:p.Asn141Ser
ENST00000296684.9:c.422A>G	ENSP00000296684.5:p.Asn141Ser
ENST00000502423.5:c.*289A>G	ENSP00000422177.1:n.*289A>G
ENST00000506765.1:c.338+12217A>G	ENSP00000424570.1:n.338+12217A>G
ENST00000506974.5:c.*198A>G	ENSP00000425967.1:n.*198A>G
ENST00000507026.5:c.*396A>G	ENSP00000424993.1:n.*396A>G
ENST00000509443.1:n.283A>G
NM_002495.2:c.422A>G	NP_002486.1:p.Asn141Ser
XM_005248525.3:c.350+12217A>G	XP_005248582.1:n.350+12217A>G
XM_011543415.1:c.248A>G	XP_011541717.1:p.Asn83Ser
NM_001318051.1:c.350+12217A>G	NP_001304980.1:n.350+12217A>G
NM_002495.3:c.422A>G	NP_002486.1:p.Asn141Ser
NR_134473.1:n.624A>G
NR_134474.1:n.541A>G
NR_134475.1:n.576A>G
NM_002495.4:c.422A>G MANE Select	NP_002486.1:p.Asn141Ser
NM_001318051.2:c.350+12217A>G	NP_001304980.1:n.350+12217A>G
NR_134473.2:n.618A>G
NR_134474.2:n.535A>G
NR_134475.2:n.570A>G