Canonical Allele Identifier: CA2673829486

Gene: NDUFS4

Linked Data

• gnomAD v4: 5-53658758-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658758T>A , CM000667.2:g.53658758T>A	GRCh38
NC_000005.9:g.52954588T>A , CM000667.1:g.52954588T>A	GRCh37
NC_000005.8:g.52990345T>A	NCBI36
NG_008200.1:g.103124T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.424+134T>A MANE Select	ENSP00000296684.5:n.424+134T>A
ENST00000296684.9:c.424+134T>A	ENSP00000296684.5:n.424+134T>A
ENST00000502423.5:c.*291+134T>A	ENSP00000422177.1:n.*291+134T>A
ENST00000506765.1:c.338+12353T>A	ENSP00000424570.1:n.338+12353T>A
ENST00000506974.5:c.*200+134T>A	ENSP00000425967.1:n.*200+134T>A
ENST00000507026.5:c.*398+134T>A	ENSP00000424993.1:n.*398+134T>A
ENST00000509443.1:n.419T>A
NM_002495.2:c.424+134T>A	NP_002486.1:n.424+134T>A
XM_005248525.3:c.350+12353T>A	XP_005248582.1:n.350+12353T>A
XM_011543415.1:c.250+134T>A	XP_011541717.1:n.250+134T>A
NM_001318051.1:c.350+12353T>A	NP_001304980.1:n.350+12353T>A
NM_002495.3:c.424+134T>A	NP_002486.1:n.424+134T>A
NR_134473.1:n.626+134T>A
NR_134474.1:n.543+134T>A
NR_134475.1:n.578+134T>A
NM_002495.4:c.424+134T>A MANE Select	NP_002486.1:n.424+134T>A
NM_001318051.2:c.350+12353T>A	NP_001304980.1:n.350+12353T>A
NR_134473.2:n.620+134T>A
NR_134474.2:n.537+134T>A
NR_134475.2:n.572+134T>A