Canonical Allele Identifier: CA444330377

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942173A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646343A>G , CM000667.2:g.53646343A>G	GRCh38
NC_000005.9:g.52942173A>G , CM000667.1:g.52942173A>G	GRCh37
NC_000005.8:g.52977930A>G	NCBI36
NG_008200.1:g.90709A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.288A>G MANE Select	ENSP00000296684.5:p.Lys96=
ENST00000296684.9:c.288A>G	ENSP00000296684.5:p.Lys96=
ENST00000502423.5:c.*155A>G	ENSP00000422177.1:n.*155A>G
ENST00000506765.1:c.276A>G	ENSP00000424570.1:p.Lys92=
ENST00000506974.5:c.*64A>G	ENSP00000425967.1:n.*64A>G
ENST00000507026.5:c.*262A>G	ENSP00000424993.1:n.*262A>G
ENST00000509443.1:n.149A>G
NM_002495.2:c.288A>G	NP_002486.1:p.Lys96=
XM_005248525.3:c.288A>G	XP_005248582.1:p.Lys96=
XM_011543415.1:c.114A>G	XP_011541717.1:p.Lys38=
NM_001318051.1:c.288A>G	NP_001304980.1:p.Lys96=
NM_002495.3:c.288A>G	NP_002486.1:p.Lys96=
NR_134473.1:n.490A>G
NR_134474.1:n.407A>G
NR_134475.1:n.442A>G
NM_002495.4:c.288A>G MANE Select	NP_002486.1:p.Lys96=
NM_001318051.2:c.288A>G	NP_001304980.1:p.Lys96=
NR_134473.2:n.484A>G
NR_134474.2:n.401A>G
NR_134475.2:n.436A>G