Canonical Allele Identifier: CA1546660834

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646294T= , CM000667.2:g.53646294T=	GRCh38
NC_000005.9:g.52942124T= , CM000667.1:g.52942124T=	GRCh37
NC_000005.8:g.52977881T=	NCBI36
NG_008200.1:g.90660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.239T= MANE Select	ENSP00000296684.5:p.Phe80=
ENST00000296684.9:c.239T=	ENSP00000296684.5:p.Phe80=
ENST00000502423.5:c.*106T=	ENSP00000422177.1:n.*106T=
ENST00000506765.1:c.227T=	ENSP00000424570.1:p.Phe76=
ENST00000506974.5:c.*15T=	ENSP00000425967.1:n.*15T=
ENST00000507026.5:c.*213T=	ENSP00000424993.1:n.*213T=
ENST00000509443.1:n.100T=
NM_002495.2:c.239T=	NP_002486.1:p.Phe80=
XM_005248525.3:c.239T=	XP_005248582.1:p.Phe80=
XM_011543415.1:c.65T=	XP_011541717.1:p.Phe22=
NM_001318051.1:c.239T=	NP_001304980.1:p.Phe80=
NM_002495.3:c.239T=	NP_002486.1:p.Phe80=
NR_134473.1:n.441T=
NR_134474.1:n.358T=
NR_134475.1:n.393T=
NM_002495.4:c.239T= MANE Select	NP_002486.1:p.Phe80=
NM_001318051.2:c.239T=	NP_001304980.1:p.Phe80=
NR_134473.2:n.435T=
NR_134474.2:n.352T=
NR_134475.2:n.387T=