Canonical Allele Identifier: CA2673829419

Gene: NDUFS4

Linked Data

• gnomAD v4: 5-53658668-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658668T>C , CM000667.2:g.53658668T>C	GRCh38
NC_000005.9:g.52954498T>C , CM000667.1:g.52954498T>C	GRCh37
NC_000005.8:g.52990255T>C	NCBI36
NG_008200.1:g.103034T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.424+44T>C MANE Select	ENSP00000296684.5:n.424+44T>C
ENST00000296684.9:c.424+44T>C	ENSP00000296684.5:n.424+44T>C
ENST00000502423.5:c.*291+44T>C	ENSP00000422177.1:n.*291+44T>C
ENST00000506765.1:c.338+12263T>C	ENSP00000424570.1:n.338+12263T>C
ENST00000506974.5:c.*200+44T>C	ENSP00000425967.1:n.*200+44T>C
ENST00000507026.5:c.*398+44T>C	ENSP00000424993.1:n.*398+44T>C
ENST00000509443.1:n.329T>C
NM_002495.2:c.424+44T>C	NP_002486.1:n.424+44T>C
XM_005248525.3:c.350+12263T>C	XP_005248582.1:n.350+12263T>C
XM_011543415.1:c.250+44T>C	XP_011541717.1:n.250+44T>C
NM_001318051.1:c.350+12263T>C	NP_001304980.1:n.350+12263T>C
NM_002495.3:c.424+44T>C	NP_002486.1:n.424+44T>C
NR_134473.1:n.626+44T>C
NR_134474.1:n.543+44T>C
NR_134475.1:n.578+44T>C
NM_002495.4:c.424+44T>C MANE Select	NP_002486.1:n.424+44T>C
NM_001318051.2:c.350+12263T>C	NP_001304980.1:n.350+12263T>C
NR_134473.2:n.620+44T>C
NR_134474.2:n.537+44T>C
NR_134475.2:n.572+44T>C