Canonical Allele Identifier: CA1546660818

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646249C= , CM000667.2:g.53646249C=	GRCh38
NC_000005.9:g.52942079C= , CM000667.1:g.52942079C=	GRCh37
NC_000005.8:g.52977836C=	NCBI36
NG_008200.1:g.90615C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.194C= MANE Select	ENSP00000296684.5:p.Thr65=
ENST00000296684.9:c.194C=	ENSP00000296684.5:p.Thr65=
ENST00000502423.5:c.*61C=	ENSP00000422177.1:n.*61C=
ENST00000506765.1:c.182C=	ENSP00000424570.1:p.Thr61=
ENST00000506974.5:c.366C=	ENSP00000425967.1:p.Asn122=
ENST00000507026.5:c.*168C=	ENSP00000424993.1:n.*168C=
ENST00000509443.1:n.55C=
NM_002495.2:c.194C=	NP_002486.1:p.Thr65=
XM_005248525.3:c.194C=	XP_005248582.1:p.Thr65=
XM_011543415.1:c.20C=	XP_011541717.1:p.Thr7=
NM_001318051.1:c.194C=	NP_001304980.1:p.Thr65=
NM_002495.3:c.194C=	NP_002486.1:p.Thr65=
NR_134473.1:n.396C=
NR_134474.1:n.313C=
NR_134475.1:n.348C=
NM_002495.4:c.194C= MANE Select	NP_002486.1:p.Thr65=
NM_001318051.2:c.194C=	NP_001304980.1:p.Thr65=
NR_134473.2:n.390C=
NR_134474.2:n.307C=
NR_134475.2:n.342C=