Canonical Allele Identifier: CA1546620689

Gene: NDUFS4

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560675T= , CM000667.2:g.53560675T=	GRCh38
NC_000005.9:g.52856505T= , CM000667.1:g.52856505T=	GRCh37
NC_000005.8:g.52892262T=	NCBI36
NG_008200.1:g.5041T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.13T= MANE Select	ENSP00000296684.5:p.Ser5=
ENST00000296684.9:c.13T=	ENSP00000296684.5:p.Ser5=
ENST00000502423.5:c.13T=	ENSP00000422177.1:p.Ser5=
ENST00000506765.1:c.1T=	ENSP00000424570.1:p.Ser1=
ENST00000506974.5:c.13T=	ENSP00000425967.1:p.Ser5=
ENST00000507026.5:c.13T=	ENSP00000424993.1:p.Ser5=
NM_002495.2:c.13T=	NP_002486.1:p.Ser5=
XM_005248525.3:c.13T=	XP_005248582.1:p.Ser5=
XM_011543414.1:c.13T=	XP_011541716.1:p.Ser5=
NM_001318051.1:c.13T=	NP_001304980.1:p.Ser5=
NM_002495.3:c.13T=	NP_002486.1:p.Ser5=
NR_134473.1:n.43T=
NR_134474.1:n.43T=
NR_134475.1:n.43T=
XM_017009491.1:c.13T=	XP_016864980.1:p.Ser5=
NM_002495.4:c.13T= MANE Select	NP_002486.1:p.Ser5=
NM_001318051.2:c.13T=	NP_001304980.1:p.Ser5=
NR_134473.2:n.37T=
NR_134474.2:n.37T=
NR_134475.2:n.37T=