Canonical Allele Identifier: CA1546660815

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646239A= , CM000667.2:g.53646239A=	GRCh38
NC_000005.9:g.52942069A= , CM000667.1:g.52942069A=	GRCh37
NC_000005.8:g.52977826A=	NCBI36
NG_008200.1:g.90605A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.184A= MANE Select	ENSP00000296684.5:p.Thr62=
ENST00000296684.9:c.184A=	ENSP00000296684.5:p.Thr62=
ENST00000502423.5:c.*51A=	ENSP00000422177.1:n.*51A=
ENST00000506765.1:c.172A=	ENSP00000424570.1:p.Thr58=
ENST00000506974.5:c.356A=	ENSP00000425967.1:p.His119=
ENST00000507026.5:c.*158A=	ENSP00000424993.1:n.*158A=
ENST00000509443.1:n.45A=
NM_002495.2:c.184A=	NP_002486.1:p.Thr62=
XM_005248525.3:c.184A=	XP_005248582.1:p.Thr62=
XM_011543415.1:c.10A=	XP_011541717.1:p.Thr4=
NM_001318051.1:c.184A=	NP_001304980.1:p.Thr62=
NM_002495.3:c.184A=	NP_002486.1:p.Thr62=
NR_134473.1:n.386A=
NR_134474.1:n.303A=
NR_134475.1:n.338A=
NM_002495.4:c.184A= MANE Select	NP_002486.1:p.Thr62=
NM_001318051.2:c.184A=	NP_001304980.1:p.Thr62=
NR_134473.2:n.380A=
NR_134474.2:n.297A=
NR_134475.2:n.332A=