Canonical Allele Identifier: CA1546666277

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658568A= , CM000667.2:g.53658568A=	GRCh38
NC_000005.9:g.52954398A= , CM000667.1:g.52954398A=	GRCh37
NC_000005.8:g.52990155A=	NCBI36
NG_008200.1:g.102934A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.368A= MANE Select	ENSP00000296684.5:p.Asn123=
ENST00000296684.9:c.368A=	ENSP00000296684.5:p.Asn123=
ENST00000502423.5:c.*235A=	ENSP00000422177.1:n.*235A=
ENST00000506765.1:c.338+12163A=	ENSP00000424570.1:n.338+12163A=
ENST00000506974.5:c.*144A=	ENSP00000425967.1:n.*144A=
ENST00000507026.5:c.*342A=	ENSP00000424993.1:n.*342A=
ENST00000509443.1:n.229A=
NM_002495.2:c.368A=	NP_002486.1:p.Asn123=
XM_005248525.3:c.350+12163A=	XP_005248582.1:n.350+12163A=
XM_011543415.1:c.194A=	XP_011541717.1:p.Asn65=
NM_001318051.1:c.350+12163A=	NP_001304980.1:n.350+12163A=
NM_002495.3:c.368A=	NP_002486.1:p.Asn123=
NR_134473.1:n.570A=
NR_134474.1:n.487A=
NR_134475.1:n.522A=
NM_002495.4:c.368A= MANE Select	NP_002486.1:p.Asn123=
NM_001318051.2:c.350+12163A=	NP_001304980.1:n.350+12163A=
NR_134473.2:n.564A=
NR_134474.2:n.481A=
NR_134475.2:n.516A=