Canonical Allele Identifier: CA1546660874

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646381A= , CM000667.2:g.53646381A=	GRCh38
NC_000005.9:g.52942211A= , CM000667.1:g.52942211A=	GRCh37
NC_000005.8:g.52977968A=	NCBI36
NG_008200.1:g.90747A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000296684.10:c.326A= MANE Select	ENSP00000296684.5:p.Asn109=
ENST00000296684.9:c.326A=	ENSP00000296684.5:p.Asn109=
ENST00000502423.5:c.*193A=	ENSP00000422177.1:n.*193A=
ENST00000506765.1:c.314A=	ENSP00000424570.1:p.Asn105=
ENST00000506974.5:c.*102A=	ENSP00000425967.1:n.*102A=
ENST00000507026.5:c.*300A=	ENSP00000424993.1:n.*300A=
ENST00000509443.1:n.187A=
NM_002495.2:c.326A=	NP_002486.1:p.Asn109=
XM_005248525.3:c.326A=	XP_005248582.1:p.Asn109=
XM_011543415.1:c.152A=	XP_011541717.1:p.Asn51=
NM_001318051.1:c.326A=	NP_001304980.1:p.Asn109=
NM_002495.3:c.326A=	NP_002486.1:p.Asn109=
NR_134473.1:n.528A=
NR_134474.1:n.445A=
NR_134475.1:n.480A=
NM_002495.4:c.326A= MANE Select	NP_002486.1:p.Asn109=
NM_001318051.2:c.326A=	NP_001304980.1:p.Asn109=
NR_134473.2:n.522A=
NR_134474.2:n.439A=
NR_134475.2:n.474A=