Canonical Allele Identifier: CA1546660857

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646344T= , CM000667.2:g.53646344T=	GRCh38
NC_000005.9:g.52942174T= , CM000667.1:g.52942174T=	GRCh37
NC_000005.8:g.52977931T=	NCBI36
NG_008200.1:g.90710T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.289T= MANE Select	ENSP00000296684.5:p.Trp97=
ENST00000296684.9:c.289T=	ENSP00000296684.5:p.Trp97=
ENST00000502423.5:c.*156T=	ENSP00000422177.1:n.*156T=
ENST00000506765.1:c.277T=	ENSP00000424570.1:p.Trp93=
ENST00000506974.5:c.*65T=	ENSP00000425967.1:n.*65T=
ENST00000507026.5:c.*263T=	ENSP00000424993.1:n.*263T=
ENST00000509443.1:n.150T=
NM_002495.2:c.289T=	NP_002486.1:p.Trp97=
XM_005248525.3:c.289T=	XP_005248582.1:p.Trp97=
XM_011543415.1:c.115T=	XP_011541717.1:p.Trp39=
NM_001318051.1:c.289T=	NP_001304980.1:p.Trp97=
NM_002495.3:c.289T=	NP_002486.1:p.Trp97=
NR_134473.1:n.491T=
NR_134474.1:n.408T=
NR_134475.1:n.443T=
NM_002495.4:c.289T= MANE Select	NP_002486.1:p.Trp97=
NM_001318051.2:c.289T=	NP_001304980.1:p.Trp97=
NR_134473.2:n.485T=
NR_134474.2:n.402T=
NR_134475.2:n.437T=