Canonical Allele Identifier: CA1546660865

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646362A= , CM000667.2:g.53646362A=	GRCh38
NC_000005.9:g.52942192A= , CM000667.1:g.52942192A=	GRCh37
NC_000005.8:g.52977949A=	NCBI36
NG_008200.1:g.90728A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.307A= MANE Select	ENSP00000296684.5:p.Thr103=
ENST00000296684.9:c.307A=	ENSP00000296684.5:p.Thr103=
ENST00000502423.5:c.*174A=	ENSP00000422177.1:n.*174A=
ENST00000506765.1:c.295A=	ENSP00000424570.1:p.Thr99=
ENST00000506974.5:c.*83A=	ENSP00000425967.1:n.*83A=
ENST00000507026.5:c.*281A=	ENSP00000424993.1:n.*281A=
ENST00000509443.1:n.168A=
NM_002495.2:c.307A=	NP_002486.1:p.Thr103=
XM_005248525.3:c.307A=	XP_005248582.1:p.Thr103=
XM_011543415.1:c.133A=	XP_011541717.1:p.Thr45=
NM_001318051.1:c.307A=	NP_001304980.1:p.Thr103=
NM_002495.3:c.307A=	NP_002486.1:p.Thr103=
NR_134473.1:n.509A=
NR_134474.1:n.426A=
NR_134475.1:n.461A=
NM_002495.4:c.307A= MANE Select	NP_002486.1:p.Thr103=
NM_001318051.2:c.307A=	NP_001304980.1:p.Thr103=
NR_134473.2:n.503A=
NR_134474.2:n.420A=
NR_134475.2:n.455A=