Canonical Allele Identifier: CA1546666204

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658412T= , CM000667.2:g.53658412T=	GRCh38
NC_000005.9:g.52954242T= , CM000667.1:g.52954242T=	GRCh37
NC_000005.8:g.52989999T=	NCBI36
NG_008200.1:g.102778T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.351-139T= MANE Select	ENSP00000296684.5:n.351-139T=
ENST00000296684.9:c.351-139T=	ENSP00000296684.5:n.351-139T=
ENST00000502423.5:c.*218-139T=	ENSP00000422177.1:n.*218-139T=
ENST00000506765.1:c.338+12007T=	ENSP00000424570.1:n.338+12007T=
ENST00000506974.5:c.*127-139T=	ENSP00000425967.1:n.*127-139T=
ENST00000507026.5:c.*325-139T=	ENSP00000424993.1:n.*325-139T=
ENST00000509443.1:n.212-139T=
NM_002495.2:c.351-139T=	NP_002486.1:n.351-139T=
XM_005248525.3:c.350+12007T=	XP_005248582.1:n.350+12007T=
XM_011543415.1:c.177-139T=	XP_011541717.1:n.177-139T=
NM_001318051.1:c.350+12007T=	NP_001304980.1:n.350+12007T=
NM_002495.3:c.351-139T=	NP_002486.1:n.351-139T=
NR_134473.1:n.553-139T=
NR_134474.1:n.470-139T=
NR_134475.1:n.505-139T=
NM_002495.4:c.351-139T= MANE Select	NP_002486.1:n.351-139T=
NM_001318051.2:c.350+12007T=	NP_001304980.1:n.350+12007T=
NR_134473.2:n.547-139T=
NR_134474.2:n.464-139T=
NR_134475.2:n.499-139T=