Canonical Allele Identifier: CA359719861

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942210A>G (hg19) ; chr5:g.53646380A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646380A>G , CM000667.2:g.53646380A>G	GRCh38
NC_000005.9:g.52942210A>G , CM000667.1:g.52942210A>G	GRCh37
NC_000005.8:g.52977967A>G	NCBI36
NG_008200.1:g.90746A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000296684.10:c.325A>G MANE Select	ENSP00000296684.5:p.Asn109Asp
ENST00000296684.9:c.325A>G	ENSP00000296684.5:p.Asn109Asp
ENST00000502423.5:c.*192A>G	ENSP00000422177.1:n.*192A>G
ENST00000506765.1:c.313A>G	ENSP00000424570.1:p.Asn105Asp
ENST00000506974.5:c.*101A>G	ENSP00000425967.1:n.*101A>G
ENST00000507026.5:c.*299A>G	ENSP00000424993.1:n.*299A>G
ENST00000509443.1:n.186A>G
NM_002495.2:c.325A>G	NP_002486.1:p.Asn109Asp
XM_005248525.3:c.325A>G	XP_005248582.1:p.Asn109Asp
XM_011543415.1:c.151A>G	XP_011541717.1:p.Asn51Asp
NM_001318051.1:c.325A>G	NP_001304980.1:p.Asn109Asp
NM_002495.3:c.325A>G	NP_002486.1:p.Asn109Asp
NR_134473.1:n.527A>G
NR_134474.1:n.444A>G
NR_134475.1:n.479A>G
NM_002495.4:c.325A>G MANE Select	NP_002486.1:p.Asn109Asp
NM_001318051.2:c.325A>G	NP_001304980.1:p.Asn109Asp
NR_134473.2:n.521A>G
NR_134474.2:n.438A>G
NR_134475.2:n.473A>G