Canonical Allele Identifier: CA444329680

Gene: NDUFS4

Linked Data

• dbSNP Id: rs936926115
• MyVariant Identifiers: chr5:g.52856507A>C (hg19) ; chr5:g.53560677A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53560677A>C , CM000667.2:g.53560677A>C	GRCh38
NC_000005.9:g.52856507A>C , CM000667.1:g.52856507A>C	GRCh37
NC_000005.8:g.52892264A>C	NCBI36
NG_008200.1:g.5043A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.15A>C MANE Select	ENSP00000296684.5:p.Ser5=
ENST00000296684.9:c.15A>C	ENSP00000296684.5:p.Ser5=
ENST00000502423.5:c.15A>C	ENSP00000422177.1:p.Ser5=
ENST00000506765.1:c.3A>C	ENSP00000424570.1:p.Ser1=
ENST00000506974.5:c.15A>C	ENSP00000425967.1:p.Ser5=
ENST00000507026.5:c.15A>C	ENSP00000424993.1:p.Ser5=
NM_002495.2:c.15A>C	NP_002486.1:p.Ser5=
XM_005248525.3:c.15A>C	XP_005248582.1:p.Ser5=
XM_011543414.1:c.15A>C	XP_011541716.1:p.Ser5=
NM_001318051.1:c.15A>C	NP_001304980.1:p.Ser5=
NM_002495.3:c.15A>C	NP_002486.1:p.Ser5=
NR_134473.1:n.45A>C
NR_134474.1:n.45A>C
NR_134475.1:n.45A>C
XM_017009491.1:c.15A>C	XP_016864980.1:p.Ser5=
NM_002495.4:c.15A>C MANE Select	NP_002486.1:p.Ser5=
NM_001318051.2:c.15A>C	NP_001304980.1:p.Ser5=
NR_134473.2:n.39A>C
NR_134474.2:n.39A>C
NR_134475.2:n.39A>C