Canonical Allele Identifier: CA359719245

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52954443C>T (hg19) ; chr5:g.53658613C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658613C>T , CM000667.2:g.53658613C>T	GRCh38
NC_000005.9:g.52954443C>T , CM000667.1:g.52954443C>T	GRCh37
NC_000005.8:g.52990200C>T	NCBI36
NG_008200.1:g.102979C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.413C>T MANE Select	ENSP00000296684.5:p.Ala138Val
ENST00000296684.9:c.413C>T	ENSP00000296684.5:p.Ala138Val
ENST00000502423.5:c.*280C>T	ENSP00000422177.1:n.*280C>T
ENST00000506765.1:c.338+12208C>T	ENSP00000424570.1:n.338+12208C>T
ENST00000506974.5:c.*189C>T	ENSP00000425967.1:n.*189C>T
ENST00000507026.5:c.*387C>T	ENSP00000424993.1:n.*387C>T
ENST00000509443.1:n.274C>T
NM_002495.2:c.413C>T	NP_002486.1:p.Ala138Val
XM_005248525.3:c.350+12208C>T	XP_005248582.1:n.350+12208C>T
XM_011543415.1:c.239C>T	XP_011541717.1:p.Ala80Val
NM_001318051.1:c.350+12208C>T	NP_001304980.1:n.350+12208C>T
NM_002495.3:c.413C>T	NP_002486.1:p.Ala138Val
NR_134473.1:n.615C>T
NR_134474.1:n.532C>T
NR_134475.1:n.567C>T
NM_002495.4:c.413C>T MANE Select	NP_002486.1:p.Ala138Val
NM_001318051.2:c.350+12208C>T	NP_001304980.1:n.350+12208C>T
NR_134473.2:n.609C>T
NR_134474.2:n.526C>T
NR_134475.2:n.561C>T