Canonical Allele Identifier: CA1546660814

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646237T= , CM000667.2:g.53646237T=	GRCh38
NC_000005.9:g.52942067T= , CM000667.1:g.52942067T=	GRCh37
NC_000005.8:g.52977824T=	NCBI36
NG_008200.1:g.90603T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.182T= MANE Select	ENSP00000296684.5:p.Ile61=
ENST00000296684.9:c.182T=	ENSP00000296684.5:p.Ile61=
ENST00000502423.5:c.*49T=	ENSP00000422177.1:n.*49T=
ENST00000506765.1:c.170T=	ENSP00000424570.1:p.Ile57=
ENST00000506974.5:c.354T=	ENSP00000425967.1:p.Tyr118=
ENST00000507026.5:c.*156T=	ENSP00000424993.1:n.*156T=
ENST00000509443.1:n.43T=
NM_002495.2:c.182T=	NP_002486.1:p.Ile61=
XM_005248525.3:c.182T=	XP_005248582.1:p.Ile61=
XM_011543415.1:c.8T=	XP_011541717.1:p.Ile3=
NM_001318051.1:c.182T=	NP_001304980.1:p.Ile61=
NM_002495.3:c.182T=	NP_002486.1:p.Ile61=
NR_134473.1:n.384T=
NR_134474.1:n.301T=
NR_134475.1:n.336T=
NM_002495.4:c.182T= MANE Select	NP_002486.1:p.Ile61=
NM_001318051.2:c.182T=	NP_001304980.1:p.Ile61=
NR_134473.2:n.378T=
NR_134474.2:n.295T=
NR_134475.2:n.330T=