Canonical Allele Identifier: CA1546660821

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646257C= , CM000667.2:g.53646257C=	GRCh38
NC_000005.9:g.52942087C= , CM000667.1:g.52942087C=	GRCh37
NC_000005.8:g.52977844C=	NCBI36
NG_008200.1:g.90623C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.202C= MANE Select	ENSP00000296684.5:p.Pro68=
ENST00000296684.9:c.202C=	ENSP00000296684.5:p.Pro68=
ENST00000502423.5:c.*69C=	ENSP00000422177.1:n.*69C=
ENST00000506765.1:c.190C=	ENSP00000424570.1:p.Pro64=
ENST00000506974.5:c.374C=	ENSP00000425967.1:p.Ser125=
ENST00000507026.5:c.*176C=	ENSP00000424993.1:n.*176C=
ENST00000509443.1:n.63C=
NM_002495.2:c.202C=	NP_002486.1:p.Pro68=
XM_005248525.3:c.202C=	XP_005248582.1:p.Pro68=
XM_011543415.1:c.28C=	XP_011541717.1:p.Pro10=
NM_001318051.1:c.202C=	NP_001304980.1:p.Pro68=
NM_002495.3:c.202C=	NP_002486.1:p.Pro68=
NR_134473.1:n.404C=
NR_134474.1:n.321C=
NR_134475.1:n.356C=
NM_002495.4:c.202C= MANE Select	NP_002486.1:p.Pro68=
NM_001318051.2:c.202C=	NP_001304980.1:p.Pro68=
NR_134473.2:n.398C=
NR_134474.2:n.315C=
NR_134475.2:n.350C=