Canonical Allele Identifier: CA444330369

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942158A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646328A>G , CM000667.2:g.53646328A>G	GRCh38
NC_000005.9:g.52942158A>G , CM000667.1:g.52942158A>G	GRCh37
NC_000005.8:g.52977915A>G	NCBI36
NG_008200.1:g.90694A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.273A>G MANE Select	ENSP00000296684.5:p.Val91=
ENST00000296684.9:c.273A>G	ENSP00000296684.5:p.Val91=
ENST00000502423.5:c.*140A>G	ENSP00000422177.1:n.*140A>G
ENST00000506765.1:c.261A>G	ENSP00000424570.1:p.Val87=
ENST00000506974.5:c.*49A>G	ENSP00000425967.1:n.*49A>G
ENST00000507026.5:c.*247A>G	ENSP00000424993.1:n.*247A>G
ENST00000509443.1:n.134A>G
NM_002495.2:c.273A>G	NP_002486.1:p.Val91=
XM_005248525.3:c.273A>G	XP_005248582.1:p.Val91=
XM_011543415.1:c.99A>G	XP_011541717.1:p.Val33=
NM_001318051.1:c.273A>G	NP_001304980.1:p.Val91=
NM_002495.3:c.273A>G	NP_002486.1:p.Val91=
NR_134473.1:n.475A>G
NR_134474.1:n.392A>G
NR_134475.1:n.427A>G
NM_002495.4:c.273A>G MANE Select	NP_002486.1:p.Val91=
NM_001318051.2:c.273A>G	NP_001304980.1:p.Val91=
NR_134473.2:n.469A>G
NR_134474.2:n.386A>G
NR_134475.2:n.421A>G