Canonical Allele Identifier: CA1546660828

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646278A= , CM000667.2:g.53646278A=	GRCh38
NC_000005.9:g.52942108A= , CM000667.1:g.52942108A=	GRCh37
NC_000005.8:g.52977865A=	NCBI36
NG_008200.1:g.90644A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.223A= MANE Select	ENSP00000296684.5:p.Arg75=
ENST00000296684.9:c.223A=	ENSP00000296684.5:p.Arg75=
ENST00000502423.5:c.*90A=	ENSP00000422177.1:n.*90A=
ENST00000506765.1:c.211A=	ENSP00000424570.1:p.Arg71=
ENST00000506974.5:c.395A=	ENSP00000425967.1:p.Ter132=
ENST00000507026.5:c.*197A=	ENSP00000424993.1:n.*197A=
ENST00000509443.1:n.84A=
NM_002495.2:c.223A=	NP_002486.1:p.Arg75=
XM_005248525.3:c.223A=	XP_005248582.1:p.Arg75=
XM_011543415.1:c.49A=	XP_011541717.1:p.Arg17=
NM_001318051.1:c.223A=	NP_001304980.1:p.Arg75=
NM_002495.3:c.223A=	NP_002486.1:p.Arg75=
NR_134473.1:n.425A=
NR_134474.1:n.342A=
NR_134475.1:n.377A=
NM_002495.4:c.223A= MANE Select	NP_002486.1:p.Arg75=
NM_001318051.2:c.223A=	NP_001304980.1:p.Arg75=
NR_134473.2:n.419A=
NR_134474.2:n.336A=
NR_134475.2:n.371A=