Canonical Allele Identifier: CA1546660847

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646323G= , CM000667.2:g.53646323G=	GRCh38
NC_000005.9:g.52942153G= , CM000667.1:g.52942153G=	GRCh37
NC_000005.8:g.52977910G=	NCBI36
NG_008200.1:g.90689G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.268G= MANE Select	ENSP00000296684.5:p.Gly90=
ENST00000296684.9:c.268G=	ENSP00000296684.5:p.Gly90=
ENST00000502423.5:c.*135G=	ENSP00000422177.1:n.*135G=
ENST00000506765.1:c.256G=	ENSP00000424570.1:p.Gly86=
ENST00000506974.5:c.*44G=	ENSP00000425967.1:n.*44G=
ENST00000507026.5:c.*242G=	ENSP00000424993.1:n.*242G=
ENST00000509443.1:n.129G=
NM_002495.2:c.268G=	NP_002486.1:p.Gly90=
XM_005248525.3:c.268G=	XP_005248582.1:p.Gly90=
XM_011543415.1:c.94G=	XP_011541717.1:p.Gly32=
NM_001318051.1:c.268G=	NP_001304980.1:p.Gly90=
NM_002495.3:c.268G=	NP_002486.1:p.Gly90=
NR_134473.1:n.470G=
NR_134474.1:n.387G=
NR_134475.1:n.422G=
NM_002495.4:c.268G= MANE Select	NP_002486.1:p.Gly90=
NM_001318051.2:c.268G=	NP_001304980.1:p.Gly90=
NR_134473.2:n.464G=
NR_134474.2:n.381G=
NR_134475.2:n.416G=