Canonical Allele Identifier: CA444330321

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942083A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646253A>G , CM000667.2:g.53646253A>G	GRCh38
NC_000005.9:g.52942083A>G , CM000667.1:g.52942083A>G	GRCh37
NC_000005.8:g.52977840A>G	NCBI36
NG_008200.1:g.90619A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.198A>G MANE Select	ENSP00000296684.5:p.Gly66=
ENST00000296684.9:c.198A>G	ENSP00000296684.5:p.Gly66=
ENST00000502423.5:c.*65A>G	ENSP00000422177.1:n.*65A>G
ENST00000506765.1:c.186A>G	ENSP00000424570.1:p.Gly62=
ENST00000506974.5:c.370A>G	ENSP00000425967.1:p.Ser124Gly
ENST00000507026.5:c.*172A>G	ENSP00000424993.1:n.*172A>G
ENST00000509443.1:n.59A>G
NM_002495.2:c.198A>G	NP_002486.1:p.Gly66=
XM_005248525.3:c.198A>G	XP_005248582.1:p.Gly66=
XM_011543415.1:c.24A>G	XP_011541717.1:p.Gly8=
NM_001318051.1:c.198A>G	NP_001304980.1:p.Gly66=
NM_002495.3:c.198A>G	NP_002486.1:p.Gly66=
NR_134473.1:n.400A>G
NR_134474.1:n.317A>G
NR_134475.1:n.352A>G
NM_002495.4:c.198A>G MANE Select	NP_002486.1:p.Gly66=
NM_001318051.2:c.198A>G	NP_001304980.1:p.Gly66=
NR_134473.2:n.394A>G
NR_134474.2:n.311A>G
NR_134475.2:n.346A>G