Canonical Allele Identifier: CA359719629

Gene: NDUFS4

Linked Data

• MyVariant Identifiers: chr5:g.52942109G>C (hg19) ; chr5:g.53646279G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53646279G>C , CM000667.2:g.53646279G>C	GRCh38
NC_000005.9:g.52942109G>C , CM000667.1:g.52942109G>C	GRCh37
NC_000005.8:g.52977866G>C	NCBI36
NG_008200.1:g.90645G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296684.10:c.224G>C MANE Select	ENSP00000296684.5:p.Arg75Thr
ENST00000296684.9:c.224G>C	ENSP00000296684.5:p.Arg75Thr
ENST00000502423.5:c.*91G>C	ENSP00000422177.1:n.*91G>C
ENST00000506765.1:c.212G>C	ENSP00000424570.1:p.Arg71Thr
ENST00000506974.5:c.396G>C	ENSP00000425967.1:p.Ter132Tyr
ENST00000507026.5:c.*198G>C	ENSP00000424993.1:n.*198G>C
ENST00000509443.1:n.85G>C
NM_002495.2:c.224G>C	NP_002486.1:p.Arg75Thr
XM_005248525.3:c.224G>C	XP_005248582.1:p.Arg75Thr
XM_011543415.1:c.50G>C	XP_011541717.1:p.Arg17Thr
NM_001318051.1:c.224G>C	NP_001304980.1:p.Arg75Thr
NM_002495.3:c.224G>C	NP_002486.1:p.Arg75Thr
NR_134473.1:n.426G>C
NR_134474.1:n.343G>C
NR_134475.1:n.378G>C
NM_002495.4:c.224G>C MANE Select	NP_002486.1:p.Arg75Thr
NM_001318051.2:c.224G>C	NP_001304980.1:p.Arg75Thr
NR_134473.2:n.420G>C
NR_134474.2:n.337G>C
NR_134475.2:n.372G>C