Canonical Allele Identifier: CA444329737

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52856561T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560731T>A , CM000667.2:g.53560731T>A	GRCh38
NC_000005.9:g.52856561T>A , CM000667.1:g.52856561T>A	GRCh37
NC_000005.8:g.52892318T>A	NCBI36
NG_008200.1:g.5097T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.69T>A MANE Select	ENSP00000296684.5:p.Ala23=
ENST00000296684.9:c.69T>A	ENSP00000296684.5:p.Ala23=
ENST00000502423.5:c.69T>A	ENSP00000422177.1:p.Ala23=
ENST00000506765.1:c.57T>A	ENSP00000424570.1:p.Ala19=
ENST00000506974.5:c.69T>A	ENSP00000425967.1:p.Ala23=
ENST00000507026.5:c.69T>A	ENSP00000424993.1:p.Ala23=
NM_002495.2:c.69T>A	NP_002486.1:p.Ala23=
XM_005248525.3:c.69T>A	XP_005248582.1:p.Ala23=
XM_011543414.1:c.69T>A	XP_011541716.1:p.Ala23=
NM_001318051.1:c.69T>A	NP_001304980.1:p.Ala23=
NM_002495.3:c.69T>A	NP_002486.1:p.Ala23=
NR_134473.1:n.99T>A
NR_134474.1:n.99T>A
NR_134475.1:n.99T>A
XM_017009491.1:c.69T>A	XP_016864980.1:p.Ala23=
NM_002495.4:c.69T>A MANE Select	NP_002486.1:p.Ala23=
NM_001318051.2:c.69T>A	NP_001304980.1:p.Ala23=
NR_134473.2:n.93T>A
NR_134474.2:n.93T>A
NR_134475.2:n.93T>A