Canonical Allele Identifier: CA1546666214

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53658436A= , CM000667.2:g.53658436A=	GRCh38
NC_000005.9:g.52954266A= , CM000667.1:g.52954266A=	GRCh37
NC_000005.8:g.52990023A=	NCBI36
NG_008200.1:g.102802A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.351-115A= MANE Select	ENSP00000296684.5:n.351-115A=
ENST00000296684.9:c.351-115A=	ENSP00000296684.5:n.351-115A=
ENST00000502423.5:c.*218-115A=	ENSP00000422177.1:n.*218-115A=
ENST00000506765.1:c.338+12031A=	ENSP00000424570.1:n.338+12031A=
ENST00000506974.5:c.*127-115A=	ENSP00000425967.1:n.*127-115A=
ENST00000507026.5:c.*325-115A=	ENSP00000424993.1:n.*325-115A=
ENST00000509443.1:n.212-115A=
NM_002495.2:c.351-115A=	NP_002486.1:n.351-115A=
XM_005248525.3:c.350+12031A=	XP_005248582.1:n.350+12031A=
XM_011543415.1:c.177-115A=	XP_011541717.1:n.177-115A=
NM_001318051.1:c.350+12031A=	NP_001304980.1:n.350+12031A=
NM_002495.3:c.351-115A=	NP_002486.1:n.351-115A=
NR_134473.1:n.553-115A=
NR_134474.1:n.470-115A=
NR_134475.1:n.505-115A=
NM_002495.4:c.351-115A= MANE Select	NP_002486.1:n.351-115A=
NM_001318051.2:c.350+12031A=	NP_001304980.1:n.350+12031A=
NR_134473.2:n.547-115A=
NR_134474.2:n.464-115A=
NR_134475.2:n.499-115A=