Canonical Allele Identifier: CA359719258

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52954449A>G (hg19) ; chr5:g.53658619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658619A>G , CM000667.2:g.53658619A>G	GRCh38
NC_000005.9:g.52954449A>G , CM000667.1:g.52954449A>G	GRCh37
NC_000005.8:g.52990206A>G	NCBI36
NG_008200.1:g.102985A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.419A>G MANE Select	ENSP00000296684.5:p.Lys140Arg
ENST00000296684.9:c.419A>G	ENSP00000296684.5:p.Lys140Arg
ENST00000502423.5:c.*286A>G	ENSP00000422177.1:n.*286A>G
ENST00000506765.1:c.338+12214A>G	ENSP00000424570.1:n.338+12214A>G
ENST00000506974.5:c.*195A>G	ENSP00000425967.1:n.*195A>G
ENST00000507026.5:c.*393A>G	ENSP00000424993.1:n.*393A>G
ENST00000509443.1:n.280A>G
NM_002495.2:c.419A>G	NP_002486.1:p.Lys140Arg
XM_005248525.3:c.350+12214A>G	XP_005248582.1:n.350+12214A>G
XM_011543415.1:c.245A>G	XP_011541717.1:p.Lys82Arg
NM_001318051.1:c.350+12214A>G	NP_001304980.1:n.350+12214A>G
NM_002495.3:c.419A>G	NP_002486.1:p.Lys140Arg
NR_134473.1:n.621A>G
NR_134474.1:n.538A>G
NR_134475.1:n.573A>G
NM_002495.4:c.419A>G MANE Select	NP_002486.1:p.Lys140Arg
NM_001318051.2:c.350+12214A>G	NP_001304980.1:n.350+12214A>G
NR_134473.2:n.615A>G
NR_134474.2:n.532A>G
NR_134475.2:n.567A>G