Canonical Allele Identifier: CA1546660764

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646166C= , CM000667.2:g.53646166C=	GRCh38
NC_000005.9:g.52941996C= , CM000667.1:g.52941996C=	GRCh37
NC_000005.8:g.52977753C=	NCBI36
NG_008200.1:g.90532C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.178-67C= MANE Select	ENSP00000296684.5:n.178-67C=
ENST00000296684.9:c.178-67C=	ENSP00000296684.5:n.178-67C=
ENST00000502423.5:c.*45-67C=	ENSP00000422177.1:n.*45-67C=
ENST00000506765.1:c.166-67C=	ENSP00000424570.1:n.166-67C=
ENST00000506974.5:c.350-67C=	ENSP00000425967.1:n.350-67C=
ENST00000507026.5:c.*152-67C=	ENSP00000424993.1:n.*152-67C=
NM_002495.2:c.178-67C=	NP_002486.1:n.178-67C=
XM_005248525.3:c.178-67C=	XP_005248582.1:n.178-67C=
XM_011543415.1:c.4-67C=	XP_011541717.1:n.4-67C=
NM_001318051.1:c.178-67C=	NP_001304980.1:n.178-67C=
NM_002495.3:c.178-67C=	NP_002486.1:n.178-67C=
NR_134473.1:n.380-67C=
NR_134474.1:n.297-67C=
NR_134475.1:n.332-67C=
NM_002495.4:c.178-67C= MANE Select	NP_002486.1:n.178-67C=
NM_001318051.2:c.178-67C=	NP_001304980.1:n.178-67C=
NR_134473.2:n.374-67C=
NR_134474.2:n.291-67C=
NR_134475.2:n.326-67C=