Canonical Allele Identifier: CA1546666237

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658489T= , CM000667.2:g.53658489T=	GRCh38
NC_000005.9:g.52954319T= , CM000667.1:g.52954319T=	GRCh37
NC_000005.8:g.52990076T=	NCBI36
NG_008200.1:g.102855T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.351-62T= MANE Select	ENSP00000296684.5:n.351-62T=
ENST00000296684.9:c.351-62T=	ENSP00000296684.5:n.351-62T=
ENST00000502423.5:c.*218-62T=	ENSP00000422177.1:n.*218-62T=
ENST00000506765.1:c.338+12084T=	ENSP00000424570.1:n.338+12084T=
ENST00000506974.5:c.*127-62T=	ENSP00000425967.1:n.*127-62T=
ENST00000507026.5:c.*325-62T=	ENSP00000424993.1:n.*325-62T=
ENST00000509443.1:n.212-62T=
NM_002495.2:c.351-62T=	NP_002486.1:n.351-62T=
XM_005248525.3:c.350+12084T=	XP_005248582.1:n.350+12084T=
XM_011543415.1:c.177-62T=	XP_011541717.1:n.177-62T=
NM_001318051.1:c.350+12084T=	NP_001304980.1:n.350+12084T=
NM_002495.3:c.351-62T=	NP_002486.1:n.351-62T=
NR_134473.1:n.553-62T=
NR_134474.1:n.470-62T=
NR_134475.1:n.505-62T=
NM_002495.4:c.351-62T= MANE Select	NP_002486.1:n.351-62T=
NM_001318051.2:c.350+12084T=	NP_001304980.1:n.350+12084T=
NR_134473.2:n.547-62T=
NR_134474.2:n.464-62T=
NR_134475.2:n.499-62T=